WNT2 (Wnt family member 2) - Rat Genome Database

Name: WNT2
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: WNT2 (Wnt family member 2) Homo sapiens

Analyze

Symbol:

WNT2

Name:

Wnt family member 2

RGD ID:

736431

HGNC Page

HGNC:12780

Description:

Enables cytokine activity and frizzled binding activity. Involved in several processes, including cellular response to transforming growth factor beta stimulus; midbrain development; and positive regulation of fibroblast proliferation. Located in collagen-containing extracellular matrix; cytoplasm; and extracellular region. Implicated in breast carcinoma; hepatocellular carcinoma; and urinary system cancer. Biomarker of breast cancer; endometrial carcinoma; and prostate cancer.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

int-1-like protein 1; Int-1-related protein; INT1L1; IRP; protein Wnt-2; secreted growth factor; wingless-related mmtv integration site 2; wingless-type MMTV integration site family member 2

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Wnt2 (wingless-type MMTV integration site family, member 2)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Rattus norvegicus (Norway rat):	Wnt2 (Wnt family member 2)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, Panther
Chinchilla lanigera (long-tailed chinchilla):	Wnt2 (Wnt family member 2)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	WNT2 (Wnt family member 2)	NCBI	Ortholog
Canis lupus familiaris (dog):	WNT2 (Wnt family member 2)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Wnt2 (Wnt family member 2)	NCBI	Ortholog
Sus scrofa (pig):	WNT2 (Wnt family member 2)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	WNT2 (Wnt family member 2)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Wnt2 (Wnt family member 2)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Wnt2 (Wnt family member 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Wnt2 (wingless-type MMTV integration site family, member 2)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	wnt2 (wingless-type MMTV integration site family member 2)	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|PhylomeDB\|ZFIN)
Xenopus laevis (African clawed frog):	wnt2.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	wnt2	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	117,275,451 - 117,323,058 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	117,275,451 - 117,323,152 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	116,915,505 - 116,963,112 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	116,704,518 - 116,750,579 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	7	116,511,232 - 116,557,294	NCBI
Celera	7	111,724,862 - 111,771,525 (-)	NCBI		Celera
Cytogenetic Map	7	q31.2	NCBI
HuRef	7	111,282,485 - 111,328,966 (-)	NCBI		HuRef
CHM1_1	7	116,850,055 - 116,896,705 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	7	118,590,786 - 118,638,396 (-)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	116,312,120 - 116,358,781 (-)	NCBI

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

autistic disorder (EXP)

breast cancer (IEP)

breast carcinoma (IAGP)

endometrial carcinoma (IEP)

Experimental Mammary Neoplasms (IDA)

Fibroadenoma (IEP)

genetic disease (IAGP)

hepatocellular carcinoma (IAGP)

pleomorphic xanthoastrocytoma (IAGP)

prostate cancer (IEP)

renal cell carcinoma (IAGP)

Renal Cell Carcinoma 1 (IAGP)

urinary system cancer (IAGP)

Uterine Cervical Neoplasms (EXP)

visual epilepsy (ISO)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(1->4)-beta-D-glucan (ISO)

1,3-dinitrobenzene (ISO)

1-nitropyrene (EXP)

17beta-estradiol (EXP,ISO)

2,3,7,8-tetrachlorodibenzodioxine (EXP,ISO)

4,4'-diaminodiphenylmethane (ISO)

4,4'-sulfonyldiphenol (ISO)

4-amino-2,6-dinitrotoluene (ISO)

5-aza-2'-deoxycytidine (EXP)

6-propyl-2-thiouracil (ISO)

afimoxifene (EXP)

all-trans-retinoic acid (EXP)

amitrole (ISO)

ammonium chloride (ISO)

antirheumatic drug (EXP)

arsenite(3-) (EXP,ISO)

benzo[a]pyrene (EXP,ISO)

bisphenol A (EXP,ISO)

bisphenol F (ISO)

cadmium dichloride (EXP)

carbon nanotube (ISO)

chloroprene (ISO)

chlorpyrifos (ISO)

clotrimazole (ISO)

cocaine (ISO)

Cuprizon (ISO)

deguelin (EXP)

dextran sulfate (ISO)

diazinon (ISO)

dichromium trioxide (EXP)

dieldrin (ISO)

dioxygen (EXP,ISO)

dorsomorphin (EXP)

doxorubicin (EXP)

entinostat (EXP)

ethanol (EXP)

ethylparaben (EXP)

finasteride (ISO)

fulvestrant (EXP)

glufosinate (ISO)

lead diacetate (EXP)

lipopolysaccharide (EXP)

methimazole (ISO)

methoxychlor (ISO)

N(gamma)-nitro-L-arginine methyl ester (ISO)

N-methyl-4-phenylpyridinium (ISO)

N-methyl-N'-nitro-N-nitrosoguanidine (EXP)

N-nitrosodiethylamine (ISO)

nickel atom (ISO)

nickel subsulfide (ISO)

nitrofen (ISO)

oxaliplatin (ISO)

ozone (ISO)

paracetamol (ISO)

paraquat (ISO)

perfluorooctane-1-sulfonic acid (ISO)

phenobarbital (ISO)

resveratrol (EXP)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

SB 431542 (EXP)

silicon dioxide (EXP)

sodium arsenite (EXP)

titanium dioxide (ISO)

topotecan (ISO)

triclosan (EXP)

triphenyl phosphate (ISO)

valproic acid (EXP,ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

atrial cardiac muscle tissue morphogenesis (IEA,ISO)

canonical Wnt signaling pathway (IBA,IDA,IEA,IMP,ISO,TAS)

cardiac epithelial to mesenchymal transition (IEA,ISO)

cardiac muscle cell proliferation (IEA,ISO)

cell fate commitment (IBA,IEA)

cell proliferation in midbrain (IDA,IEA)

cell-cell signaling (IDA)

cellular response to retinoic acid (ISS)

cellular response to transforming growth factor beta stimulus (IEP)

epithelial cell proliferation (IEA,ISO)

epithelial cell proliferation involved in lung morphogenesis (IEA,ISO)

iris morphogenesis (ISS)

labyrinthine layer blood vessel development (IEA,ISO)

lens development in camera-type eye (ISS)

lung development (ISO)

lung induction (IEA,ISO)

mammary gland epithelium development (IEP)

mesenchymal cell proliferation (IEA,ISO)

midbrain dopaminergic neuron differentiation (IDA)

neurogenesis (TAS)

neuron differentiation (IBA,IEA,ISS)

positive regulation of cardiac muscle cell proliferation (IEA,ISO)

positive regulation of cell population proliferation (IDA)

positive regulation of endothelial cell proliferation (ISO)

positive regulation of epithelial cell proliferation (IEA,ISO)

positive regulation of epithelial cell proliferation involved in lung morphogenesis (IEA,ISO)

positive regulation of fibroblast proliferation (IMP)

positive regulation of mesenchymal cell proliferation (IEA,ISO)

positive regulation of neurogenesis (IEA)

positive regulation of transcription by RNA polymerase II (IDA,IEA,ISO)

system development (IEA)

Wnt signaling pathway (IEA,ISO)

Cellular Component

collagen-containing extracellular matrix (IDA)

cytoplasm (IDA)

extracellular region (IDA,IEA,NAS,TAS)

extracellular space (IBA,IEA)

Wnt signalosome (IC)

Molecular Function

cytokine activity (IBA,IDA,IEA)

frizzled binding (IBA,IEA,IPI)

protein binding (IPI)

receptor ligand activity (IDA,IMP)

signaling receptor binding (IEA)

Molecular Pathway Annotations Click to see Annotation Detail View

basal cell carcinoma pathway (IEA)

Hedgehog signaling pathway (IEA)

Wnt signaling pathway (IEA,TAS)

Wnt signaling, canonical pathway (TAS)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Delayed speech and language development (IAGP)

Papillary renal cell carcinoma type 1 (IAGP)

Pleomorphic xanthoastrocytoma (IAGP)

Renal cell carcinoma (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	Expression and hormone regulation of Wnt2, 3, 4, 5a, 7a, 7b and 10b in normal human endometrium and endometrial carcinoma.	Bui TD, etal., Br J Cancer. 1997;75(8):1131-6.
2.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
3.	Oncogene amplification in urothelial cancers with p53 gene mutation or MDM2 amplification.	Habuchi T, etal., J Natl Cancer Inst. 1994 Sep 7;86(17):1331-5.
4.	Differential expression of human Wnt genes 2, 3, 4, and 7B in human breast cell lines and normal and disease states of human breast tissue.	Huguet EL, etal., Cancer Res. 1994 May 15;54(10):2615-21.
5.	Influence of polymorphisms in the Wnt/β-catenin pathway genes on hepatocellular carcinoma risk in a Chinese Han population.	Li QM, etal., Medicine (Baltimore). 2017 Mar;96(12):e6127. doi: 10.1097/MD.0000000000006127.
6.	Chronic electroconvulsive seizure up-regulates beta-catenin expression in rat hippocampus: role in adult neurogenesis.	Madsen TM, etal., Biol Psychiatry. 2003 Nov 15;54(10):1006-14.
7.	Analysis of genetic alterations related to the development and progression of breast carcinoma.	Nagayama K and Watatani M, Jpn J Cancer Res. 1993 Nov;84(11):1159-64.
8.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
9.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
10.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
11.	The Wnt Homepage	Roel Nusse - Howard Hughes Medical Institute and the Department of Developmental Biology at Stanford University, California, USA
12.	Transformation by Wnt family proteins correlates with regulation of beta-catenin.	Shimizu H, etal., Cell Growth Differ. 1997 Dec;8(12):1349-58.
13.	Alternative wnt signaling is initiated by distinct receptors.	van Amerongen R, etal., Sci Signal. 2008 Sep 2;1(35):re9.
14.	Expression of twist and wnt in human breast cancer.	Watanabe O, etal., Anticancer Res. 2004 Nov-Dec;24(6):3851-6.
15.	WIF1, a component of the Wnt pathway, is down-regulated in prostate, breast, lung, and bladder cancer.	Wissmann C, etal., J Pathol 2003 Oct;201(2):204-12.
16.	Differential transformation of mammary epithelial cells by Wnt genes.	Wong GT, etal., Mol Cell Biol. 1994 Sep;14(9):6278-86.

Additional References at PubMed

PMID:1846319	PMID:2971536	PMID:8167409	PMID:10347172	PMID:10557084	PMID:11290296	PMID:11449391	PMID:11712082	PMID:11840514	PMID:12063568	PMID:12138115	PMID:12147710
PMID:12477932	PMID:12690205	PMID:12853948	PMID:14533014	PMID:14702039	PMID:15040835	PMID:15048648	PMID:15489334	PMID:15507471	PMID:15878915	PMID:15896469	PMID:15900580
PMID:16132582	PMID:16258938	PMID:16407829	PMID:17386109	PMID:17534895	PMID:17948129	PMID:18184402	PMID:18600204	PMID:18703315	PMID:18949017	PMID:19038973	PMID:19058789
PMID:19239325	PMID:19421142	PMID:19444628	PMID:19666519	PMID:19734317	PMID:19857041	PMID:19895723	PMID:19913121	PMID:20018874	PMID:20492734	PMID:20628086	PMID:20628624
PMID:21474991	PMID:21575668	PMID:21732829	PMID:21873635	PMID:21988832	PMID:22041457	PMID:22489561	PMID:22522212	PMID:22763454	PMID:22872573	PMID:22949635	PMID:23250740
PMID:23268410	PMID:23322712	PMID:23603171	PMID:23610556	PMID:23694962	PMID:23815780	PMID:24431302	PMID:25472883	PMID:25731618	PMID:26116230	PMID:26186194	PMID:26484565
PMID:26968103	PMID:27336854	PMID:27513465	PMID:28081867	PMID:28514442	PMID:28553956	PMID:28627774	PMID:28631286	PMID:28656880	PMID:28665975	PMID:29109390	PMID:29259372
PMID:30594543	PMID:30945288	PMID:32779546	PMID:33155209	PMID:33961781	PMID:34274970	PMID:34375306	PMID:34477243	PMID:34666560	PMID:34862305	PMID:35037695

Genomics

Comparative Map Data

WNT2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	117,275,451 - 117,323,058 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	117,275,451 - 117,323,152 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	116,915,505 - 116,963,112 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	116,704,518 - 116,750,579 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	7	116,511,232 - 116,557,294	NCBI
Celera	7	111,724,862 - 111,771,525 (-)	NCBI		Celera
Cytogenetic Map	7	q31.2	NCBI
HuRef	7	111,282,485 - 111,328,966 (-)	NCBI		HuRef
CHM1_1	7	116,850,055 - 116,896,705 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	7	118,590,786 - 118,638,396 (-)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	116,312,120 - 116,358,781 (-)	NCBI

Wnt2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	6	17,988,939 - 18,032,771 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	6	17,988,939 - 18,030,584 (-)	Ensembl		GRCm39 Ensembl
GRCm38	6	17,985,474 - 18,032,772 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	6	17,988,940 - 18,030,585 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	6	17,938,940 - 17,980,445 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	6	17,938,940 - 17,980,356 (-)	NCBI		MGSCv36	mm8
Celera	6	18,070,129 - 18,111,436 (-)	NCBI		Celera
Cytogenetic Map	6	A2	NCBI
cM Map	6	8.08	NCBI

Wnt2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	4	47,294,300 - 47,340,284 (-)	NCBI		GRCr8
mRatBN7.2	4	46,328,408 - 46,374,673 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	4	46,333,998 - 46,374,402 (-)	Ensembl		mRatBN7.2 Ensembl
Rnor_6.0	4	45,286,845 - 45,332,899 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	4	45,292,437 - 45,332,420 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	4	45,892,395 - 45,936,605 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	4	43,649,783 - 43,689,596 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	4	43,857,074 - 43,859,488 (-)	NCBI
Celera	4	41,596,263 - 41,642,309 (-)	NCBI		Celera
Cytogenetic Map	4	q22	NCBI

Wnt2
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955432	22,984,170 - 23,027,705 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955432	22,988,208 - 23,024,530 (-)	NCBI	ChiLan1.0	ChiLan1.0

WNT2
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	6	154,101,025 - 154,151,405 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	7	6,111,284 - 6,161,665 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	7	109,244,772 - 109,291,472 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	7	121,939,254 - 121,985,862 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	7	121,936,031 - 121,985,862 (-)	Ensembl	panpan1.1		panPan2

WNT2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	14	56,123,735 - 56,172,113 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	14	56,129,248 - 56,172,069 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	14	55,519,061 - 55,567,484 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	14	56,163,101 - 56,211,441 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	14	56,166,256 - 56,213,190 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	14	56,195,055 - 56,243,473 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	14	55,884,128 - 55,931,047 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	14	56,253,933 - 56,302,214 (-)	NCBI		UU_Cfam_GSD_1.0

Wnt2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024405118	44,819,573 - 44,865,128 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936589	1,825,209 - 1,866,889 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936589	1,825,209 - 1,866,898 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

WNT2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	18	28,946,326 - 28,993,961 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	18	28,945,825 - 28,993,969 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	18	30,790,071 - 30,838,269 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

WNT2
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	21	85,955,517 - 86,005,664 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	21	85,955,145 - 86,001,730 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666042	17,730,443 - 17,777,632 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Wnt2
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624827	2,045,595 - 2,089,442 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624827	2,045,733 - 2,088,284 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in WNT2
14 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1	copy number loss	See cases [RCV000052250]	Chr7:53985..159282531 [GRCh38] Chr7:53985..159075220 [GRCh37] Chr7:149068..158767981 [NCBI36] Chr7:7p22.3-q36.3	pathogenic
GRCh38/hg38 7q31.1-31.31(chr7:110524677-118306203)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054159]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054159]\|See cases [RCV000054159]	Chr7:110524677..118306203 [GRCh38] Chr7:110164734..117946257 [GRCh37] Chr7:109951970..117733493 [NCBI36] Chr7:7q31.1-31.31	pathogenic
GRCh38/hg38 7q31.1-31.33(chr7:113799835-124899218)x1	copy number loss	See cases [RCV000054160]	Chr7:113799835..124899218 [GRCh38] Chr7:113439890..124539272 [GRCh37] Chr7:113227126..124326508 [NCBI36] Chr7:7q31.1-31.33	pathogenic
NM_003391.2(WNT2):c.505C>T (p.Arg169Cys)	single nucleotide variant	Malignant melanoma [RCV000061539]	Chr7:117315154 [GRCh38] Chr7:116955208 [GRCh37] Chr7:116742444 [NCBI36] Chr7:7q31.2	not provided
NM_003391.2(WNT2):c.853+2448G>A	single nucleotide variant	Lung cancer [RCV000105443]	Chr7:117295164 [GRCh38] Chr7:116935218 [GRCh37] Chr7:7q31.2	uncertain significance
GRCh38/hg38 7q31.1-31.33(chr7:114142477-125840381)x1	copy number loss	See cases [RCV000135311]	Chr7:114142477..125840381 [GRCh38] Chr7:113782532..125480435 [GRCh37] Chr7:113569768..125267671 [NCBI36] Chr7:7q31.1-31.33	pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	copy number loss	See cases [RCV000135401]	Chr7:54185..159282390 [GRCh38] Chr7:54185..159075079 [GRCh37] Chr7:149268..158767840 [NCBI36] Chr7:7p22.3-q36.3	pathogenic
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3	copy number gain	See cases [RCV000136717]	Chr7:97419852..158923762 [GRCh38] Chr7:97049164..158716453 [GRCh37] Chr7:96887100..158409214 [NCBI36] Chr7:7q21.3-36.3	pathogenic
GRCh38/hg38 7q22.1-31.31(chr7:102196924-121278641)x1	copy number loss	See cases [RCV000137522]	Chr7:102196924..121278641 [GRCh38] Chr7:101912320..120918695 [GRCh37] Chr7:101626924..120705931 [NCBI36] Chr7:7q22.1-31.31	pathogenic
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3	copy number gain	See cases [RCV000141413]	Chr7:115459015..159325817 [GRCh38] Chr7:115099069..159118507 [GRCh37] Chr7:114886305..158811268 [NCBI36] Chr7:7q31.2-36.3	pathogenic
GRCh38/hg38 7q31.1-31.31(chr7:114898882-117790123)x1	copy number loss	See cases [RCV000142459]	Chr7:114898882..117790123 [GRCh38] Chr7:114538937..117430177 [GRCh37] Chr7:114326173..117217413 [NCBI36] Chr7:7q31.1-31.31	pathogenic
GRCh37/hg19 7q31.1-32.1(chr7:111613396-127897316)x1	copy number loss	See cases [RCV000240177]	Chr7:111613396..127897316 [GRCh37] Chr7:7q31.1-32.1	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1	copy number loss	See cases [RCV000446044]	Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
TMEM106B-BRAF fusion	deletion	Pleomorphic xanthoastrocytoma [RCV000454357]	Chr7:12258147..140494267 [GRCh37] Chr7:7p21.3-q34	pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3	copy number gain	See cases [RCV000447709]	Chr7:98969247..159119707 [GRCh37] Chr7:7q22.1-36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)	copy number gain	See cases [RCV000510686]	Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3	copy number gain	See cases [RCV000511549]	Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7q31.1-31.31(chr7:113764678-117694762)x3	copy number gain	See cases [RCV000511301]	Chr7:113764678..117694762 [GRCh37] Chr7:7q31.1-31.31	uncertain significance
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3	copy number gain	not provided [RCV000682911]	Chr7:98693388..159119707 [GRCh37] Chr7:7q22.1-36.3	pathogenic
GRCh37/hg19 7q31.2-31.31(chr7:115520087-118098306)x1	copy number loss	not provided [RCV000682899]	Chr7:115520087..118098306 [GRCh37] Chr7:7q31.2-31.31	likely pathogenic
NC_000007.13:g.(?_116339129)_(117144427_?)dup	duplication	Papillary renal cell carcinoma type 1 [RCV000707756]	Chr7:116699075..117504373 [GRCh38] Chr7:116339129..117144427 [GRCh37] Chr7:7q31.2	uncertain significance
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3	copy number gain	not provided [RCV000746280]	Chr7:44935..159126310 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3	copy number gain	not provided [RCV000746278]	Chr7:10704..159122532 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3	copy number gain	not provided [RCV000848126]	Chr7:10365..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
NM_003391.3(WNT2):c.792G>A (p.Thr264=)	single nucleotide variant	not provided [RCV000954435]	Chr7:117297673 [GRCh38] Chr7:116937727 [GRCh37] Chr7:7q31.2	benign
GRCh37/hg19 7q31.1-31.31(chr7:107410314-117825549)x1	copy number loss	not provided [RCV000846765]	Chr7:107410314..117825549 [GRCh37] Chr7:7q31.1-31.31	pathogenic
NM_003391.3(WNT2):c.1057A>G (p.Asn353Asp)	single nucleotide variant	not provided [RCV000892838]	Chr7:117278181 [GRCh38] Chr7:116918235 [GRCh37] Chr7:7q31.2	benign
GRCh37/hg19 7q22.3-31.32(chr7:106617406-123217914)x1	copy number loss	not provided [RCV001005991]	Chr7:106617406..123217914 [GRCh37] Chr7:7q22.3-31.32	pathogenic
NM_003391.3(WNT2):c.187C>T (p.Arg63Cys)	single nucleotide variant	Inborn genetic diseases [RCV003274631]	Chr7:117320690 [GRCh38] Chr7:116960744 [GRCh37] Chr7:7q31.2	uncertain significance
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3	copy number gain	not provided [RCV001005994]	Chr7:109251060..159119707 [GRCh37] Chr7:7q31.1-36.3	pathogenic
NC_000007.14:g.(?_116699075)_(117667118_?)del	deletion	Papillary renal cell carcinoma type 1 [RCV001032957]	Chr7:116339129..117307172 [GRCh37] Chr7:7q31.2	uncertain significance
Single allele	complex	Ring chromosome 7 [RCV002280646]	Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7q31.2-31.33(chr7:116297277-126370694)	copy number loss	Global developmental delay [RCV001352642]	Chr7:116297277..126370694 [GRCh37] Chr7:7q31.2-31.33	pathogenic
NC_000007.13:g.(?_116339139)_(117307162_?)del	deletion	Renal cell carcinoma [RCV001343585]	Chr7:116339139..117307162 [GRCh37] Chr7:7q31.2	uncertain significance
GRCh37/hg19 7q22.1-31.31(chr7:100676872-119156160)	copy number loss	not specified [RCV002053712]	Chr7:100676872..119156160 [GRCh37] Chr7:7q22.1-31.31	pathogenic
GRCh37/hg19 7q22.3-32.1(chr7:106984287-128949489)	copy number gain	not specified [RCV002053715]	Chr7:106984287..128949489 [GRCh37] Chr7:7q22.3-32.1	pathogenic
Single allele	deletion	Delayed speech and language development [RCV002251690]	Chr7:114888786..124720929 [GRCh37] Chr7:7q31.2-31.33	likely pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1	copy number loss	See cases [RCV002287832]	Chr7:56604613..96692931 [GRCh37] Chr7:7p22.3-q36.3	uncertain significance
NM_003391.3(WNT2):c.506G>A (p.Arg169His)	single nucleotide variant	Inborn genetic diseases [RCV002772618]	Chr7:117315153 [GRCh38] Chr7:116955207 [GRCh37] Chr7:7q31.2	uncertain significance
NM_003391.3(WNT2):c.418A>G (p.Lys140Glu)	single nucleotide variant	Inborn genetic diseases [RCV002738193]	Chr7:117315241 [GRCh38] Chr7:116955295 [GRCh37] Chr7:7q31.2	uncertain significance
NM_003391.3(WNT2):c.913G>A (p.Glu305Lys)	single nucleotide variant	Inborn genetic diseases [RCV002804926]	Chr7:117278325 [GRCh38] Chr7:116918379 [GRCh37] Chr7:7q31.2	uncertain significance
NM_003391.3(WNT2):c.317G>A (p.Arg106Gln)	single nucleotide variant	Inborn genetic diseases [RCV002641190]	Chr7:117315342 [GRCh38] Chr7:116955396 [GRCh37] Chr7:7q31.2	uncertain significance
NM_003391.3(WNT2):c.731T>C (p.Val244Ala)	single nucleotide variant	Inborn genetic diseases [RCV002898086]	Chr7:117297734 [GRCh38] Chr7:116937788 [GRCh37] Chr7:7q31.2	uncertain significance
NM_003391.3(WNT2):c.203G>C (p.Gly68Ala)	single nucleotide variant	Inborn genetic diseases [RCV002879288]	Chr7:117320674 [GRCh38] Chr7:116960728 [GRCh37] Chr7:7q31.2	uncertain significance
GRCh38/hg38 7q31.2(chr7:116868268-117565389)	copy number gain	Anomalous pulmonary venous return [RCV003223570]	Chr7:116868268..117565389 [GRCh38] Chr7:7q31.2	uncertain significance
GRCh37/hg19 7q31.2(chr7:116747524-116975763)x3	copy number gain	not provided [RCV003484700]	Chr7:116747524..116975763 [GRCh37] Chr7:7q31.2	uncertain significance
GRCh38/hg38 7q31.1-31.2(chr7:113604778-117643891)	copy number loss	Autism spectrum disorder [RCV003883405]	Chr7:113604778..117643891 [GRCh38] Chr7:7q31.1-31.2	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1508
Count of miRNA genes:	753
Interacting mature miRNAs:	858
Transcripts:	ENST00000265441, ENST00000449446, ENST00000461427, ENST00000491214
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region

G49397

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,962,962 - 116,963,074	UniSTS	GRCh37
Build 36	7	116,750,198 - 116,750,310	RGD	NCBI36
Celera	7	111,771,144 - 111,771,256	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,328,585 - 111,328,697	UniSTS
CRA_TCAGchr7v2	7	116,358,400 - 116,358,512	UniSTS

D7S23

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,963,409 - 116,963,714	UniSTS	GRCh37
GRCh37	7	116,988,629 - 116,988,834	UniSTS	GRCh37
GRCh37	7	116,988,046 - 116,989,001	UniSTS	GRCh37
GRCh37	7	116,989,870 - 116,990,276	UniSTS	GRCh37
GRCh37	7	116,963,397 - 116,963,726	UniSTS	GRCh37
GRCh37	7	116,929,201 - 116,929,491	UniSTS	GRCh37
GRCh37	7	116,962,555 - 116,962,661	UniSTS	GRCh37
GRCh37	7	116,928,705 - 116,929,715	UniSTS	GRCh37
Build 36	7	116,716,437 - 116,716,727	RGD	NCBI36
Celera	7	111,796,228 - 111,797,183	UniSTS
Celera	7	111,771,591 - 111,771,896	UniSTS
Celera	7	111,796,811 - 111,797,016	UniSTS
Celera	7	111,736,889 - 111,737,899	UniSTS
Celera	7	111,770,735 - 111,770,843	UniSTS
Celera	7	111,798,052 - 111,798,458	UniSTS
Celera	7	111,737,385 - 111,737,675	RGD
Celera	7	111,771,579 - 111,771,908	UniSTS
HuRef	7	111,328,176 - 111,328,284	UniSTS
HuRef	7	111,329,020 - 111,329,349	UniSTS
HuRef	7	111,355,493 - 111,355,899	UniSTS
HuRef	7	111,329,032 - 111,329,337	UniSTS
HuRef	7	111,295,025 - 111,295,315	UniSTS
HuRef	7	111,353,669 - 111,354,624	UniSTS
HuRef	7	111,354,252 - 111,354,457	UniSTS
HuRef	7	111,294,529 - 111,295,539	UniSTS
CRA_TCAGchr7v2	7	116,384,067 - 116,384,272	UniSTS
CRA_TCAGchr7v2	7	116,383,484 - 116,384,439	UniSTS
CRA_TCAGchr7v2	7	116,357,991 - 116,358,099	UniSTS
CRA_TCAGchr7v2	7	116,324,144 - 116,325,154	UniSTS
CRA_TCAGchr7v2	7	116,324,640 - 116,324,930	UniSTS
CRA_TCAGchr7v2	7	116,358,847 - 116,359,152	UniSTS
CRA_TCAGchr7v2	7	116,385,308 - 116,385,714	UniSTS
CRA_TCAGchr7v2	7	116,358,835 - 116,359,164	UniSTS

RH17465

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,442 - 116,917,574	UniSTS	GRCh37
Build 36	7	116,704,678 - 116,704,810	RGD	NCBI36
Celera	7	111,725,620 - 111,725,752	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,283,243 - 111,283,375	UniSTS
CRA_TCAGchr7v2	7	116,312,878 - 116,313,010	UniSTS
GeneMap99-GB4 RH Map	7	547.69	UniSTS
NCBI RH Map	7	1114.5	UniSTS

WNT2_738

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,243 - 116,918,030	UniSTS	GRCh37
Build 36	7	116,704,479 - 116,705,266	RGD	NCBI36
Celera	7	111,725,421 - 111,726,208	RGD
HuRef	7	111,283,044 - 111,283,831	UniSTS
CRA_TCAGchr7v2	7	116,312,679 - 116,313,466	UniSTS

ECD00272

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,953,441 - 116,954,358	UniSTS	GRCh37
Build 36	7	116,740,677 - 116,741,594	RGD	NCBI36
Celera	7	111,761,622 - 111,762,539	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,319,062 - 111,319,979	UniSTS
CRA_TCAGchr7v2	7	116,348,878 - 116,349,795	UniSTS

ECD00452

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,946,367 - 116,947,272	UniSTS	GRCh37
Build 36	7	116,733,603 - 116,734,508	RGD	NCBI36
Celera	7	111,754,548 - 111,755,453	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,311,988 - 111,312,893	UniSTS
CRA_TCAGchr7v2	7	116,341,804 - 116,342,709	UniSTS

ECD00896

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,952,477 - 116,953,362	UniSTS	GRCh37
Build 36	7	116,739,713 - 116,740,598	RGD	NCBI36
Celera	7	111,760,658 - 111,761,543	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,318,098 - 111,318,983	UniSTS
CRA_TCAGchr7v2	7	116,347,914 - 116,348,799	UniSTS

ECD01527

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,933,245 - 116,934,107	UniSTS	GRCh37
Build 36	7	116,720,481 - 116,721,343	RGD	NCBI36
Celera	7	111,741,429 - 111,742,291	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,298,869 - 111,299,731	UniSTS
CRA_TCAGchr7v2	7	116,328,684 - 116,329,546	UniSTS

ECD03869

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,123 - 116,917,904	UniSTS	GRCh37
Build 36	7	116,704,359 - 116,705,140	RGD	NCBI36
Celera	7	111,725,300 - 111,726,082	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,282,923 - 111,283,705	UniSTS
CRA_TCAGchr7v2	7	116,312,558 - 116,313,340	UniSTS

ECD03870

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,919,595 - 116,920,376	UniSTS	GRCh37
Build 36	7	116,706,831 - 116,707,612	RGD	NCBI36
Celera	7	111,727,773 - 111,728,554	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,285,396 - 111,286,177	UniSTS
CRA_TCAGchr7v2	7	116,315,031 - 116,315,812	UniSTS

ECD03979

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,943,241 - 116,944,019	UniSTS	GRCh37
Build 36	7	116,730,477 - 116,731,255	RGD	NCBI36
Celera	7	111,751,425 - 111,752,203	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,308,865 - 111,309,643	UniSTS
CRA_TCAGchr7v2	7	116,338,681 - 116,339,459	UniSTS

ECD04601

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,918,813 - 116,919,572	UniSTS	GRCh37
Build 36	7	116,706,049 - 116,706,808	RGD	NCBI36
Celera	7	111,726,991 - 111,727,750	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,284,614 - 111,285,373	UniSTS
CRA_TCAGchr7v2	7	116,314,249 - 116,315,008	UniSTS

ECD04678

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,961 - 116,918,718	UniSTS	GRCh37
Build 36	7	116,705,197 - 116,705,954	RGD	NCBI36
Celera	7	111,726,139 - 111,726,896	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,283,762 - 111,284,519	UniSTS
CRA_TCAGchr7v2	7	116,313,397 - 116,314,154	UniSTS

ECD05057

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,916,342 - 116,917,088	UniSTS	GRCh37
Build 36	7	116,703,578 - 116,704,324	RGD	NCBI36
Celera	7	111,724,519 - 111,725,265	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,282,142 - 111,282,888	UniSTS
CRA_TCAGchr7v2	7	116,311,777 - 116,312,523	UniSTS

ECD05093

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,963,970 - 116,964,715	UniSTS	GRCh37
Build 36	7	116,751,206 - 116,751,951	RGD	NCBI36
Celera	7	111,772,152 - 111,772,897	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,329,593 - 111,330,338	UniSTS
CRA_TCAGchr7v2	7	116,359,408 - 116,360,153	UniSTS

ECD05797

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,963,193 - 116,963,919	UniSTS	GRCh37
Build 36	7	116,750,429 - 116,751,155	RGD	NCBI36
Celera	7	111,771,375 - 111,772,101	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,328,816 - 111,329,542	UniSTS
CRA_TCAGchr7v2	7	116,358,631 - 116,359,357	UniSTS

ECD05830

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,931,066 - 116,931,791	UniSTS	GRCh37
Build 36	7	116,718,302 - 116,719,027	RGD	NCBI36
Celera	7	111,739,250 - 111,739,975	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,296,890 - 111,297,615	UniSTS
CRA_TCAGchr7v2	7	116,326,505 - 116,327,230	UniSTS

ECD06293

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,955,974 - 116,956,686	UniSTS	GRCh37
Build 36	7	116,743,210 - 116,743,922	RGD	NCBI36
Celera	7	111,764,155 - 111,764,867	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,321,595 - 111,322,307	UniSTS
CRA_TCAGchr7v2	7	116,351,411 - 116,352,123	UniSTS

ECD06931

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,955,259 - 116,955,954	UniSTS	GRCh37
Build 36	7	116,742,495 - 116,743,190	RGD	NCBI36
Celera	7	111,763,440 - 111,764,135	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,320,880 - 111,321,575	UniSTS
CRA_TCAGchr7v2	7	116,350,696 - 116,351,391	UniSTS

ECD07289

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,948,256 - 116,948,941	UniSTS	GRCh37
Build 36	7	116,735,492 - 116,736,177	RGD	NCBI36
Celera	7	111,756,437 - 111,757,122	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,313,877 - 111,314,562	UniSTS
CRA_TCAGchr7v2	7	116,343,693 - 116,344,378	UniSTS

ECD07997

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,937,549 - 116,938,215	UniSTS	GRCh37
Build 36	7	116,724,785 - 116,725,451	RGD	NCBI36
Celera	7	111,745,732 - 111,746,398	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,303,172 - 111,303,838	UniSTS
CRA_TCAGchr7v2	7	116,332,988 - 116,333,654	UniSTS

ECD08234

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,961,240 - 116,961,900	UniSTS	GRCh37
Build 36	7	116,748,476 - 116,749,136	RGD	NCBI36
Celera	7	111,769,420 - 111,770,080	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,326,861 - 111,327,521	UniSTS
CRA_TCAGchr7v2	7	116,356,676 - 116,357,336	UniSTS

ECD08601

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,947,554 - 116,948,204	UniSTS	GRCh37
Build 36	7	116,734,790 - 116,735,440	RGD	NCBI36
Celera	7	111,755,735 - 111,756,385	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,313,175 - 111,313,825	UniSTS
CRA_TCAGchr7v2	7	116,342,991 - 116,343,641	UniSTS

ECD09415

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,924,030 - 116,924,659	UniSTS	GRCh37
Build 36	7	116,711,266 - 116,711,895	RGD	NCBI36
Celera	7	111,732,211 - 111,732,840	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,289,834 - 111,290,463	UniSTS
CRA_TCAGchr7v2	7	116,319,469 - 116,320,098	UniSTS

ECD09534

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,954,515 - 116,955,141	UniSTS	GRCh37
Build 36	7	116,741,751 - 116,742,377	RGD	NCBI36
Celera	7	111,762,696 - 111,763,322	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,320,136 - 111,320,762	UniSTS
CRA_TCAGchr7v2	7	116,349,952 - 116,350,578	UniSTS

ECD09577

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,960,569 - 116,961,194	UniSTS	GRCh37
Build 36	7	116,747,805 - 116,748,430	RGD	NCBI36
Celera	7	111,768,749 - 111,769,374	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,326,190 - 111,326,815	UniSTS
CRA_TCAGchr7v2	7	116,356,005 - 116,356,630	UniSTS

ECD09948

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,961,925 - 116,962,540	UniSTS	GRCh37
Build 36	7	116,749,161 - 116,749,776	RGD	NCBI36
Celera	7	111,770,105 - 111,770,720	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,327,546 - 111,328,161	UniSTS
CRA_TCAGchr7v2	7	116,357,361 - 116,357,976	UniSTS

ECD10127

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,956,733 - 116,957,343	UniSTS	GRCh37
Build 36	7	116,743,969 - 116,744,579	RGD	NCBI36
Celera	7	111,764,914 - 111,765,524	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,322,354 - 111,322,964	UniSTS
CRA_TCAGchr7v2	7	116,352,170 - 116,352,780	UniSTS

ECD10300

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,923,383 - 116,923,988	UniSTS	GRCh37
Build 36	7	116,710,619 - 116,711,224	RGD	NCBI36
Celera	7	111,731,564 - 111,732,169	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,289,187 - 111,289,792	UniSTS
CRA_TCAGchr7v2	7	116,318,822 - 116,319,427	UniSTS

ECD11491

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,925,852 - 116,926,422	UniSTS	GRCh37
Build 36	7	116,713,088 - 116,713,658	RGD	NCBI36
Celera	7	111,734,033 - 111,734,603	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,291,656 - 111,292,226	UniSTS
CRA_TCAGchr7v2	7	116,321,291 - 116,321,861	UniSTS

ECD11734

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,944,814 - 116,945,377	UniSTS	GRCh37
Build 36	7	116,732,050 - 116,732,613	RGD	NCBI36
Celera	7	111,752,995 - 111,753,558	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,310,435 - 111,310,998	UniSTS
CRA_TCAGchr7v2	7	116,340,251 - 116,340,814	UniSTS

ECD12264

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,934,262 - 116,934,810	UniSTS	GRCh37
Build 36	7	116,721,498 - 116,722,046	RGD	NCBI36
Celera	7	111,742,446 - 111,742,993	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,299,886 - 111,300,433	UniSTS
CRA_TCAGchr7v2	7	116,329,701 - 116,330,249	UniSTS

ECD12608

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,936,114 - 116,936,653	UniSTS	GRCh37
Build 36	7	116,723,350 - 116,723,889	RGD	NCBI36
Celera	7	111,744,297 - 111,744,836	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,301,737 - 111,302,276	UniSTS
CRA_TCAGchr7v2	7	116,331,553 - 116,332,092	UniSTS

ECD12609

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,936,721 - 116,937,260	UniSTS	GRCh37
Build 36	7	116,723,957 - 116,724,496	RGD	NCBI36
Celera	7	111,744,904 - 111,745,443	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,302,344 - 111,302,883	UniSTS
CRA_TCAGchr7v2	7	116,332,160 - 116,332,699	UniSTS

ECD12676

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,926,543 - 116,927,080	UniSTS	GRCh37
Build 36	7	116,713,779 - 116,714,316	RGD	NCBI36
Celera	7	111,734,724 - 111,735,264	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,292,347 - 111,292,904	UniSTS
CRA_TCAGchr7v2	7	116,321,982 - 116,322,519	UniSTS

ECD13132

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,938,988 - 116,939,513	UniSTS	GRCh37
Build 36	7	116,726,224 - 116,726,749	RGD	NCBI36
Celera	7	111,747,171 - 111,747,696	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,304,611 - 111,305,136	UniSTS
CRA_TCAGchr7v2	7	116,334,427 - 116,334,952	UniSTS

ECD13449

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,957,511 - 116,958,028	UniSTS	GRCh37
Build 36	7	116,744,747 - 116,745,264	RGD	NCBI36
Celera	7	111,765,692 - 111,766,208	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,323,132 - 111,323,649	UniSTS
CRA_TCAGchr7v2	7	116,352,948 - 116,353,464	UniSTS

ECD13857

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,959,443 - 116,959,950	UniSTS	GRCh37
Build 36	7	116,746,679 - 116,747,186	RGD	NCBI36
Celera	7	111,767,623 - 111,768,130	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,325,064 - 111,325,571	UniSTS
CRA_TCAGchr7v2	7	116,354,879 - 116,355,386	UniSTS

ECD13932

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,928,594 - 116,929,099	UniSTS	GRCh37
Build 36	7	116,715,830 - 116,716,335	RGD	NCBI36
Celera	7	111,736,778 - 111,737,283	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,294,418 - 111,294,923	UniSTS
CRA_TCAGchr7v2	7	116,324,033 - 116,324,538	UniSTS

ECD14096

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,958,857 - 116,959,358	UniSTS	GRCh37
Build 36	7	116,746,093 - 116,746,594	RGD	NCBI36
Celera	7	111,767,037 - 111,767,538	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,324,478 - 111,324,979	UniSTS
CRA_TCAGchr7v2	7	116,354,293 - 116,354,794	UniSTS

ECD15277

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,928,083 - 116,928,557	UniSTS	GRCh37
Build 36	7	116,715,319 - 116,715,793	RGD	NCBI36
Celera	7	111,736,267 - 111,736,741	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,293,907 - 111,294,381	UniSTS
CRA_TCAGchr7v2	7	116,323,522 - 116,323,996	UniSTS

ECD15278

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,962,646 - 116,963,120	UniSTS	GRCh37
Build 36	7	116,749,882 - 116,750,356	RGD	NCBI36
Celera	7	111,770,828 - 111,771,302	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,328,269 - 111,328,743	UniSTS
CRA_TCAGchr7v2	7	116,358,084 - 116,358,558	UniSTS

ECD15603

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,958,069 - 116,958,535	UniSTS	GRCh37
Build 36	7	116,745,305 - 116,745,771	RGD	NCBI36
Celera	7	111,766,249 - 111,766,715	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,323,690 - 111,324,156	UniSTS
CRA_TCAGchr7v2	7	116,353,505 - 116,353,971	UniSTS

ECD17122

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,932,585 - 116,932,997	UniSTS	GRCh37
Build 36	7	116,719,821 - 116,720,233	RGD	NCBI36
Celera	7	111,740,769 - 111,741,181	RGD
Cytogenetic Map	7	q31.2	UniSTS
CRA_TCAGchr7v2	7	116,328,024 - 116,328,436	UniSTS

ECD17820

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,925,101 - 116,925,484	UniSTS	GRCh37
Build 36	7	116,712,337 - 116,712,720	RGD	NCBI36
Celera	7	111,733,282 - 111,733,665	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,290,905 - 111,291,288	UniSTS
CRA_TCAGchr7v2	7	116,320,540 - 116,320,923	UniSTS

ECD18534

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,941,161 - 116,941,517	UniSTS	GRCh37
Build 36	7	116,728,397 - 116,728,753	RGD	NCBI36
Celera	7	111,749,345 - 111,749,701	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,306,785 - 111,307,141	UniSTS
CRA_TCAGchr7v2	7	116,336,601 - 116,336,957	UniSTS

ECD19271

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,935,468 - 116,935,795	UniSTS	GRCh37
Build 36	7	116,722,704 - 116,723,031	RGD	NCBI36
Celera	7	111,743,651 - 111,743,978	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,301,091 - 111,301,418	UniSTS
CRA_TCAGchr7v2	7	116,330,907 - 116,331,234	UniSTS

ECD19914

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,938,539 - 116,938,843	UniSTS	GRCh37
Build 36	7	116,725,775 - 116,726,079	RGD	NCBI36
Celera	7	111,746,722 - 111,747,026	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,304,162 - 111,304,466	UniSTS
CRA_TCAGchr7v2	7	116,333,978 - 116,334,282	UniSTS

ECD20215

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,950,670 - 116,950,962	UniSTS	GRCh37
Build 36	7	116,737,906 - 116,738,198	RGD	NCBI36
Celera	7	111,758,851 - 111,759,143	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,316,291 - 111,316,583	UniSTS
CRA_TCAGchr7v2	7	116,346,107 - 116,346,399	UniSTS

ECD20239

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,949,698 - 116,949,989	UniSTS	GRCh37
Build 36	7	116,736,934 - 116,737,225	RGD	NCBI36
Celera	7	111,757,879 - 111,758,170	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,315,319 - 111,315,610	UniSTS
CRA_TCAGchr7v2	7	116,345,135 - 116,345,426	UniSTS

ECD20905

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,945,890 - 116,946,157	UniSTS	GRCh37
Build 36	7	116,733,126 - 116,733,393	RGD	NCBI36
Celera	7	111,754,071 - 111,754,338	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,311,511 - 111,311,778	UniSTS
CRA_TCAGchr7v2	7	116,341,327 - 116,341,594	UniSTS

ECD21036

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,951,118 - 116,951,381	UniSTS	GRCh37
Build 36	7	116,738,354 - 116,738,617	RGD	NCBI36
Celera	7	111,759,299 - 111,759,562	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,316,739 - 111,317,002	UniSTS
CRA_TCAGchr7v2	7	116,346,555 - 116,346,818	UniSTS

ECD21065

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,930,464 - 116,930,726	UniSTS	GRCh37
Build 36	7	116,717,700 - 116,717,962	RGD	NCBI36
Celera	7	111,738,648 - 111,738,910	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,296,288 - 111,296,550	UniSTS
CRA_TCAGchr7v2	7	116,325,903 - 116,326,165	UniSTS

ECD21103

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,960,098 - 116,960,359	UniSTS	GRCh37
Build 36	7	116,747,334 - 116,747,595	RGD	NCBI36
Celera	7	111,768,278 - 111,768,539	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,325,719 - 111,325,980	UniSTS
CRA_TCAGchr7v2	7	116,355,534 - 116,355,795	UniSTS

ECD21820

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,951,867 - 116,952,105	UniSTS	GRCh37
Build 36	7	116,739,103 - 116,739,341	RGD	NCBI36
Celera	7	111,760,048 - 111,760,286	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,317,488 - 111,317,726	UniSTS
CRA_TCAGchr7v2	7	116,347,304 - 116,347,542	UniSTS

ECD21851

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,927,422 - 116,927,659	UniSTS	GRCh37
Build 36	7	116,714,658 - 116,714,895	RGD	NCBI36
Celera	7	111,735,606 - 111,735,843	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,293,246 - 111,293,483	UniSTS
CRA_TCAGchr7v2	7	116,322,861 - 116,323,098	UniSTS

ECD22159

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,921,600 - 116,921,827	UniSTS	GRCh37
Build 36	7	116,708,836 - 116,709,063	RGD	NCBI36
Celera	7	111,729,778 - 111,730,005	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,287,401 - 111,287,628	UniSTS
CRA_TCAGchr7v2	7	116,317,036 - 116,317,263	UniSTS

ECD22292

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,929,424 - 116,929,647	UniSTS	GRCh37
Build 36	7	116,716,660 - 116,716,883	RGD	NCBI36
Celera	7	111,737,608 - 111,737,831	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,295,248 - 111,295,471	UniSTS
CRA_TCAGchr7v2	7	116,324,863 - 116,325,086	UniSTS

ECD22483

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,921,064 - 116,921,281	UniSTS	GRCh37
Build 36	7	116,708,300 - 116,708,517	RGD	NCBI36
Celera	7	111,729,242 - 111,729,459	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,286,865 - 111,287,082	UniSTS
CRA_TCAGchr7v2	7	116,316,500 - 116,316,717	UniSTS

ECD23429

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,932,150 - 116,932,339	UniSTS	GRCh37
Build 36	7	116,719,386 - 116,719,575	RGD	NCBI36
Celera	7	111,740,334 - 111,740,523	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,297,974 - 111,298,163	UniSTS
CRA_TCAGchr7v2	7	116,327,589 - 116,327,778	UniSTS

ECD24038

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,950,151 - 116,950,314	UniSTS	GRCh37
Build 36	7	116,737,387 - 116,737,550	RGD	NCBI36
Celera	7	111,758,332 - 111,758,495	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,315,772 - 111,315,935	UniSTS
CRA_TCAGchr7v2	7	116,345,588 - 116,345,751	UniSTS

ECD24187

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,949,335 - 116,949,489	UniSTS	GRCh37
Build 36	7	116,736,571 - 116,736,725	RGD	NCBI36
Celera	7	111,757,516 - 111,757,670	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,314,956 - 111,315,110	UniSTS
CRA_TCAGchr7v2	7	116,344,772 - 116,344,926	UniSTS

D7S2769

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,372 - 116,917,701	UniSTS	GRCh37
Build 36	7	116,704,608 - 116,704,937	RGD	NCBI36
Celera	7	111,725,550 - 111,725,879	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,283,173 - 111,283,502	UniSTS
CRA_TCAGchr7v2	7	116,312,808 - 116,313,137	UniSTS
Stanford-G3 RH Map	7	5748.0	UniSTS
Whitehead-YAC Contig Map	7		UniSTS
NCBI RH Map	7	1114.5	UniSTS
GeneMap99-G3 RH Map	7	5748.0	UniSTS

REN63940

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,964,898 - 116,965,143	UniSTS	GRCh37
Build 36	7	116,752,134 - 116,752,379	RGD	NCBI36
Celera	7	111,773,080 - 111,773,325	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,330,521 - 111,330,766	UniSTS
CRA_TCAGchr7v2	7	116,360,336 - 116,360,581	UniSTS

REN63941

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,964,662 - 116,964,908	UniSTS	GRCh37
Build 36	7	116,751,898 - 116,752,144	RGD	NCBI36
Celera	7	111,772,844 - 111,773,090	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,330,285 - 111,330,531	UniSTS
CRA_TCAGchr7v2	7	116,360,100 - 116,360,346	UniSTS

REN63942

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,964,421 - 116,964,653	UniSTS	GRCh37
Build 36	7	116,751,657 - 116,751,889	RGD	NCBI36
Celera	7	111,772,603 - 111,772,835	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,330,044 - 111,330,276	UniSTS
CRA_TCAGchr7v2	7	116,359,859 - 116,360,091	UniSTS

REN63943

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,964,155 - 116,964,412	UniSTS	GRCh37
Build 36	7	116,751,391 - 116,751,648	RGD	NCBI36
Celera	7	111,772,337 - 111,772,594	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,329,778 - 111,330,035	UniSTS
CRA_TCAGchr7v2	7	116,359,593 - 116,359,850	UniSTS

REN63944

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,963,914 - 116,964,169	UniSTS	GRCh37
Build 36	7	116,751,150 - 116,751,405	RGD	NCBI36
Celera	7	111,772,096 - 111,772,351	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,329,537 - 111,329,792	UniSTS
CRA_TCAGchr7v2	7	116,359,352 - 116,359,607	UniSTS

REN63945

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,963,683 - 116,963,917	UniSTS	GRCh37
Build 36	7	116,750,919 - 116,751,153	RGD	NCBI36
Celera	7	111,771,865 - 111,772,099	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,329,306 - 111,329,540	UniSTS
CRA_TCAGchr7v2	7	116,359,121 - 116,359,355	UniSTS

REN63946

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,963,437 - 116,963,683	UniSTS	GRCh37
Build 36	7	116,750,673 - 116,750,919	RGD	NCBI36
Celera	7	111,771,619 - 111,771,865	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,329,060 - 111,329,306	UniSTS
CRA_TCAGchr7v2	7	116,358,875 - 116,359,121	UniSTS

REN63947

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,963,200 - 116,963,440	UniSTS	GRCh37
Build 36	7	116,750,436 - 116,750,676	RGD	NCBI36
Celera	7	111,771,382 - 111,771,622	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,328,823 - 111,329,063	UniSTS
CRA_TCAGchr7v2	7	116,358,638 - 116,358,878	UniSTS

REN63948

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,962,988 - 116,963,219	UniSTS	GRCh37
Build 36	7	116,750,224 - 116,750,455	RGD	NCBI36
Celera	7	111,771,170 - 111,771,401	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,328,611 - 111,328,842	UniSTS
CRA_TCAGchr7v2	7	116,358,426 - 116,358,657	UniSTS

REN63949

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,962,773 - 116,963,006	UniSTS	GRCh37
Build 36	7	116,750,009 - 116,750,242	RGD	NCBI36
Celera	7	111,770,955 - 111,771,188	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,328,396 - 111,328,629	UniSTS
CRA_TCAGchr7v2	7	116,358,211 - 116,358,444	UniSTS

REN63950

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,962,561 - 116,962,790	UniSTS	GRCh37
Build 36	7	116,749,797 - 116,750,026	RGD	NCBI36
Celera	7	111,770,741 - 111,770,972	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,328,182 - 111,328,413	UniSTS
CRA_TCAGchr7v2	7	116,357,997 - 116,358,228	UniSTS

REN63951

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,962,315 - 116,962,539	UniSTS	GRCh37
Build 36	7	116,749,551 - 116,749,775	RGD	NCBI36
Celera	7	111,770,495 - 111,770,719	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,327,936 - 111,328,160	UniSTS
CRA_TCAGchr7v2	7	116,357,751 - 116,357,975	UniSTS

REN63952

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,962,095 - 116,962,319	UniSTS	GRCh37
Build 36	7	116,749,331 - 116,749,555	RGD	NCBI36
Celera	7	111,770,275 - 111,770,499	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,327,716 - 111,327,940	UniSTS
CRA_TCAGchr7v2	7	116,357,531 - 116,357,755	UniSTS

REN63953

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,961,858 - 116,962,083	UniSTS	GRCh37
Build 36	7	116,749,094 - 116,749,319	RGD	NCBI36
Celera	7	111,770,038 - 111,770,263	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,327,479 - 111,327,704	UniSTS
CRA_TCAGchr7v2	7	116,357,294 - 116,357,519	UniSTS

REN63954

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,961,574 - 116,961,841	UniSTS	GRCh37
Build 36	7	116,748,810 - 116,749,077	RGD	NCBI36
Celera	7	111,769,754 - 111,770,021	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,327,195 - 111,327,462	UniSTS
CRA_TCAGchr7v2	7	116,357,010 - 116,357,277	UniSTS

REN63955

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,961,338 - 116,961,587	UniSTS	GRCh37
Build 36	7	116,748,574 - 116,748,823	RGD	NCBI36
Celera	7	111,769,518 - 111,769,767	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,326,959 - 111,327,208	UniSTS
CRA_TCAGchr7v2	7	116,356,774 - 116,357,023	UniSTS

REN63956

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,961,092 - 116,961,346	UniSTS	GRCh37
Build 36	7	116,748,328 - 116,748,582	RGD	NCBI36
Celera	7	111,769,272 - 111,769,526	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,326,713 - 111,326,967	UniSTS
CRA_TCAGchr7v2	7	116,356,528 - 116,356,782	UniSTS

REN63957

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,960,858 - 116,961,100	UniSTS	GRCh37
Build 36	7	116,748,094 - 116,748,336	RGD	NCBI36
Celera	7	111,769,038 - 111,769,280	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,326,479 - 111,326,721	UniSTS
CRA_TCAGchr7v2	7	116,356,294 - 116,356,536	UniSTS

REN63958

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,960,651 - 116,960,877	UniSTS	GRCh37
Build 36	7	116,747,887 - 116,748,113	RGD	NCBI36
Celera	7	111,768,831 - 111,769,057	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,326,272 - 111,326,498	UniSTS
CRA_TCAGchr7v2	7	116,356,087 - 116,356,313	UniSTS

REN63959

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,960,375 - 116,960,624	UniSTS	GRCh37
Build 36	7	116,747,611 - 116,747,860	RGD	NCBI36
Celera	7	111,768,555 - 111,768,804	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,325,996 - 111,326,245	UniSTS
CRA_TCAGchr7v2	7	116,355,811 - 116,356,060	UniSTS

REN63960

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,960,123 - 116,960,385	UniSTS	GRCh37
Build 36	7	116,747,359 - 116,747,621	RGD	NCBI36
Celera	7	111,768,303 - 111,768,565	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,325,744 - 111,326,006	UniSTS
CRA_TCAGchr7v2	7	116,355,559 - 116,355,821	UniSTS

REN63961

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,959,892 - 116,960,140	UniSTS	GRCh37
Build 36	7	116,747,128 - 116,747,376	RGD	NCBI36
Celera	7	111,768,072 - 111,768,320	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,325,513 - 111,325,761	UniSTS
CRA_TCAGchr7v2	7	116,355,328 - 116,355,576	UniSTS

REN63962

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,959,659 - 116,959,905	UniSTS	GRCh37
Build 36	7	116,746,895 - 116,747,141	RGD	NCBI36
Celera	7	111,767,839 - 111,768,085	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,325,280 - 111,325,526	UniSTS
CRA_TCAGchr7v2	7	116,355,095 - 116,355,341	UniSTS

REN63963

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,959,426 - 116,959,651	UniSTS	GRCh37
Build 36	7	116,746,662 - 116,746,887	RGD	NCBI36
Celera	7	111,767,606 - 111,767,831	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,325,047 - 111,325,272	UniSTS
CRA_TCAGchr7v2	7	116,354,862 - 116,355,087	UniSTS

REN63964

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,959,169 - 116,959,400	UniSTS	GRCh37
Build 36	7	116,746,405 - 116,746,636	RGD	NCBI36
Celera	7	111,767,349 - 111,767,580	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,324,790 - 111,325,021	UniSTS
CRA_TCAGchr7v2	7	116,354,605 - 116,354,836	UniSTS

REN63965

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,958,944 - 116,959,183	UniSTS	GRCh37
Build 36	7	116,746,180 - 116,746,419	RGD	NCBI36
Celera	7	111,767,124 - 111,767,363	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,324,565 - 111,324,804	UniSTS
CRA_TCAGchr7v2	7	116,354,380 - 116,354,619	UniSTS

REN63966

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,958,648 - 116,958,885	UniSTS	GRCh37
Build 36	7	116,745,884 - 116,746,121	RGD	NCBI36
Celera	7	111,766,828 - 111,767,065	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,324,269 - 111,324,506	UniSTS
CRA_TCAGchr7v2	7	116,354,084 - 116,354,321	UniSTS

REN63967

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,958,388 - 116,958,630	UniSTS	GRCh37
Build 36	7	116,745,624 - 116,745,866	RGD	NCBI36
Celera	7	111,766,568 - 111,766,810	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,324,009 - 111,324,251	UniSTS
CRA_TCAGchr7v2	7	116,353,824 - 116,354,066	UniSTS

REN63968

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,958,064 - 116,958,324	UniSTS	GRCh37
Build 36	7	116,745,300 - 116,745,560	RGD	NCBI36
Celera	7	111,766,244 - 111,766,504	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,323,685 - 111,323,945	UniSTS
CRA_TCAGchr7v2	7	116,353,500 - 116,353,760	UniSTS

REN63969

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,957,847 - 116,958,075	UniSTS	GRCh37
Build 36	7	116,745,083 - 116,745,311	RGD	NCBI36
Celera	7	111,766,027 - 111,766,255	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,323,468 - 111,323,696	UniSTS
CRA_TCAGchr7v2	7	116,353,283 - 116,353,511	UniSTS

REN63970

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,957,596 - 116,957,820	UniSTS	GRCh37
Build 36	7	116,744,832 - 116,745,056	RGD	NCBI36
Celera	7	111,765,776 - 111,766,000	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,323,217 - 111,323,441	UniSTS
CRA_TCAGchr7v2	7	116,353,032 - 116,353,256	UniSTS

REN63971

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,957,371 - 116,957,595	UniSTS	GRCh37
Build 36	7	116,744,607 - 116,744,831	RGD	NCBI36
Celera	7	111,765,552 - 111,765,775	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,322,992 - 111,323,216	UniSTS
CRA_TCAGchr7v2	7	116,352,808 - 116,353,031	UniSTS

REN63972

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,957,122 - 116,957,354	UniSTS	GRCh37
Build 36	7	116,744,358 - 116,744,590	RGD	NCBI36
Celera	7	111,765,303 - 111,765,535	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,322,743 - 111,322,975	UniSTS
CRA_TCAGchr7v2	7	116,352,559 - 116,352,791	UniSTS

REN63973

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,956,870 - 116,957,117	UniSTS	GRCh37
Build 36	7	116,744,106 - 116,744,353	RGD	NCBI36
Celera	7	111,765,051 - 111,765,298	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,322,491 - 111,322,738	UniSTS
CRA_TCAGchr7v2	7	116,352,307 - 116,352,554	UniSTS

REN63974

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,956,659 - 116,956,889	UniSTS	GRCh37
Build 36	7	116,743,895 - 116,744,125	RGD	NCBI36
Celera	7	111,764,840 - 111,765,070	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,322,280 - 111,322,510	UniSTS
CRA_TCAGchr7v2	7	116,352,096 - 116,352,326	UniSTS

REN63975

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,956,407 - 116,956,649	UniSTS	GRCh37
Build 36	7	116,743,643 - 116,743,885	RGD	NCBI36
Celera	7	111,764,588 - 111,764,830	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,322,028 - 111,322,270	UniSTS
CRA_TCAGchr7v2	7	116,351,844 - 116,352,086	UniSTS

REN63976

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,956,171 - 116,956,395	UniSTS	GRCh37
Build 36	7	116,743,407 - 116,743,631	RGD	NCBI36
Celera	7	111,764,352 - 111,764,576	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,321,792 - 111,322,016	UniSTS
CRA_TCAGchr7v2	7	116,351,608 - 116,351,832	UniSTS

REN63977

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,955,911 - 116,956,140	UniSTS	GRCh37
Build 36	7	116,743,147 - 116,743,376	RGD	NCBI36
Celera	7	111,764,092 - 111,764,321	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,321,532 - 111,321,761	UniSTS
CRA_TCAGchr7v2	7	116,351,348 - 116,351,577	UniSTS

REN63978

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,955,672 - 116,955,897	UniSTS	GRCh37
Build 36	7	116,742,908 - 116,743,133	RGD	NCBI36
Celera	7	111,763,853 - 111,764,078	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,321,293 - 111,321,518	UniSTS
CRA_TCAGchr7v2	7	116,351,109 - 116,351,334	UniSTS

REN63979

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,955,418 - 116,955,642	UniSTS	GRCh37
Build 36	7	116,742,654 - 116,742,878	RGD	NCBI36
Celera	7	111,763,599 - 111,763,823	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,321,039 - 111,321,263	UniSTS
CRA_TCAGchr7v2	7	116,350,855 - 116,351,079	UniSTS

REN63980

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,955,186 - 116,955,413	UniSTS	GRCh37
Build 36	7	116,742,422 - 116,742,649	RGD	NCBI36
Celera	7	111,763,367 - 111,763,594	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,320,807 - 111,321,034	UniSTS
CRA_TCAGchr7v2	7	116,350,623 - 116,350,850	UniSTS

REN63981

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,954,966 - 116,955,204	UniSTS	GRCh37
Build 36	7	116,742,202 - 116,742,440	RGD	NCBI36
Celera	7	111,763,147 - 111,763,385	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,320,587 - 111,320,825	UniSTS
CRA_TCAGchr7v2	7	116,350,403 - 116,350,641	UniSTS

REN63982

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,954,728 - 116,954,959	UniSTS	GRCh37
Build 36	7	116,741,964 - 116,742,195	RGD	NCBI36
Celera	7	111,762,909 - 111,763,140	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,320,349 - 111,320,580	UniSTS
CRA_TCAGchr7v2	7	116,350,165 - 116,350,396	UniSTS

REN63983

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,954,462 - 116,954,718	UniSTS	GRCh37
Build 36	7	116,741,698 - 116,741,954	RGD	NCBI36
Celera	7	111,762,643 - 111,762,899	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,320,083 - 111,320,339	UniSTS
CRA_TCAGchr7v2	7	116,349,899 - 116,350,155	UniSTS

REN63984

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,954,237 - 116,954,463	UniSTS	GRCh37
Build 36	7	116,741,473 - 116,741,699	RGD	NCBI36
Celera	7	111,762,418 - 111,762,644	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,319,858 - 111,320,084	UniSTS
CRA_TCAGchr7v2	7	116,349,674 - 116,349,900	UniSTS

REN63985

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,953,978 - 116,954,203	UniSTS	GRCh37
Build 36	7	116,741,214 - 116,741,439	RGD	NCBI36
Celera	7	111,762,159 - 111,762,384	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,319,599 - 111,319,824	UniSTS
CRA_TCAGchr7v2	7	116,349,415 - 116,349,640	UniSTS

REN63986

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,953,762 - 116,953,995	UniSTS	GRCh37
Build 36	7	116,740,998 - 116,741,231	RGD	NCBI36
Celera	7	111,761,943 - 111,762,176	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,319,383 - 111,319,616	UniSTS
CRA_TCAGchr7v2	7	116,349,199 - 116,349,432	UniSTS

REN63987

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,953,498 - 116,953,737	UniSTS	GRCh37
Build 36	7	116,740,734 - 116,740,973	RGD	NCBI36
Celera	7	111,761,679 - 111,761,918	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,319,119 - 111,319,358	UniSTS
CRA_TCAGchr7v2	7	116,348,935 - 116,349,174	UniSTS

REN63988

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,953,259 - 116,953,496	UniSTS	GRCh37
Build 36	7	116,740,495 - 116,740,732	RGD	NCBI36
Celera	7	111,761,440 - 111,761,677	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,318,880 - 111,319,117	UniSTS
CRA_TCAGchr7v2	7	116,348,696 - 116,348,933	UniSTS

REN63989

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,953,043 - 116,953,275	UniSTS	GRCh37
Build 36	7	116,740,279 - 116,740,511	RGD	NCBI36
Celera	7	111,761,224 - 111,761,456	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,318,664 - 111,318,896	UniSTS
CRA_TCAGchr7v2	7	116,348,480 - 116,348,712	UniSTS

REN63990

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,952,765 - 116,953,022	UniSTS	GRCh37
Build 36	7	116,740,001 - 116,740,258	RGD	NCBI36
Celera	7	111,760,946 - 111,761,203	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,318,386 - 111,318,643	UniSTS
CRA_TCAGchr7v2	7	116,348,202 - 116,348,459	UniSTS

REN63991

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,952,521 - 116,952,748	UniSTS	GRCh37
Build 36	7	116,739,757 - 116,739,984	RGD	NCBI36
Celera	7	111,760,702 - 111,760,929	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,318,142 - 111,318,369	UniSTS
CRA_TCAGchr7v2	7	116,347,958 - 116,348,185	UniSTS

REN63992

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,952,300 - 116,952,534	UniSTS	GRCh37
Build 36	7	116,739,536 - 116,739,770	RGD	NCBI36
Celera	7	111,760,481 - 111,760,715	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,317,921 - 111,318,155	UniSTS
CRA_TCAGchr7v2	7	116,347,737 - 116,347,971	UniSTS

REN63993

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,952,069 - 116,952,294	UniSTS	GRCh37
Build 36	7	116,739,305 - 116,739,530	RGD	NCBI36
Celera	7	111,760,250 - 111,760,475	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,317,690 - 111,317,915	UniSTS
CRA_TCAGchr7v2	7	116,347,506 - 116,347,731	UniSTS

REN63994

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,951,747 - 116,951,975	UniSTS	GRCh37
Build 36	7	116,738,983 - 116,739,211	RGD	NCBI36
Celera	7	111,759,928 - 111,760,156	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,317,368 - 111,317,596	UniSTS
CRA_TCAGchr7v2	7	116,347,184 - 116,347,412	UniSTS

REN63995

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,951,498 - 116,951,724	UniSTS	GRCh37
Build 36	7	116,738,734 - 116,738,960	RGD	NCBI36
Celera	7	111,759,679 - 111,759,905	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,317,119 - 111,317,345	UniSTS
CRA_TCAGchr7v2	7	116,346,935 - 116,347,161	UniSTS

REN63996

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,951,218 - 116,951,444	UniSTS	GRCh37
Build 36	7	116,738,454 - 116,738,680	RGD	NCBI36
Celera	7	111,759,399 - 111,759,625	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,316,839 - 111,317,065	UniSTS
CRA_TCAGchr7v2	7	116,346,655 - 116,346,881	UniSTS

REN63997

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,950,957 - 116,951,211	UniSTS	GRCh37
Build 36	7	116,738,193 - 116,738,447	RGD	NCBI36
Celera	7	111,759,138 - 111,759,392	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,316,578 - 111,316,832	UniSTS
CRA_TCAGchr7v2	7	116,346,394 - 116,346,648	UniSTS

REN63998

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,950,732 - 116,950,965	UniSTS	GRCh37
Build 36	7	116,737,968 - 116,738,201	RGD	NCBI36
Celera	7	111,758,913 - 111,759,146	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,316,353 - 111,316,586	UniSTS
CRA_TCAGchr7v2	7	116,346,169 - 116,346,402	UniSTS

REN63999

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,950,476 - 116,950,731	UniSTS	GRCh37
Build 36	7	116,737,712 - 116,737,967	RGD	NCBI36
Celera	7	111,758,657 - 111,758,912	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,316,097 - 111,316,352	UniSTS
CRA_TCAGchr7v2	7	116,345,913 - 116,346,168	UniSTS

REN64000

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,950,145 - 116,950,375	UniSTS	GRCh37
Build 36	7	116,737,381 - 116,737,611	RGD	NCBI36
Celera	7	111,758,326 - 111,758,556	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,315,766 - 111,315,996	UniSTS
CRA_TCAGchr7v2	7	116,345,582 - 116,345,812	UniSTS

REN64001

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,949,592 - 116,949,832	UniSTS	GRCh37
Build 36	7	116,736,828 - 116,737,068	RGD	NCBI36
Celera	7	111,757,773 - 111,758,013	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,315,213 - 111,315,453	UniSTS
CRA_TCAGchr7v2	7	116,345,029 - 116,345,269	UniSTS

REN64002

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,949,351 - 116,949,601	UniSTS	GRCh37
Build 36	7	116,736,587 - 116,736,837	RGD	NCBI36
Celera	7	111,757,532 - 111,757,782	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,314,972 - 111,315,222	UniSTS
CRA_TCAGchr7v2	7	116,344,788 - 116,345,038	UniSTS

REN64003

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,949,121 - 116,949,360	UniSTS	GRCh37
Build 36	7	116,736,357 - 116,736,596	RGD	NCBI36
Celera	7	111,757,302 - 111,757,541	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,314,742 - 111,314,981	UniSTS
CRA_TCAGchr7v2	7	116,344,558 - 116,344,797	UniSTS

REN64004

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,948,863 - 116,949,121	UniSTS	GRCh37
Build 36	7	116,736,099 - 116,736,357	RGD	NCBI36
Celera	7	111,757,044 - 111,757,302	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,314,484 - 111,314,742	UniSTS
CRA_TCAGchr7v2	7	116,344,300 - 116,344,558	UniSTS

REN64005

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,948,528 - 116,948,784	UniSTS	GRCh37
Build 36	7	116,735,764 - 116,736,020	RGD	NCBI36
Celera	7	111,756,709 - 111,756,965	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,314,149 - 111,314,405	UniSTS
CRA_TCAGchr7v2	7	116,343,965 - 116,344,221	UniSTS

REN64006

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,948,302 - 116,948,538	UniSTS	GRCh37
Build 36	7	116,735,538 - 116,735,774	RGD	NCBI36
Celera	7	111,756,483 - 111,756,719	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,313,923 - 111,314,159	UniSTS
CRA_TCAGchr7v2	7	116,343,739 - 116,343,975	UniSTS

REN64007

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,948,095 - 116,948,321	UniSTS	GRCh37
Build 36	7	116,735,331 - 116,735,557	RGD	NCBI36
Celera	7	111,756,276 - 111,756,502	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,313,716 - 111,313,942	UniSTS
CRA_TCAGchr7v2	7	116,343,532 - 116,343,758	UniSTS

REN64008

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,947,839 - 116,948,073	UniSTS	GRCh37
Build 36	7	116,735,075 - 116,735,309	RGD	NCBI36
Celera	7	111,756,020 - 111,756,254	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,313,460 - 111,313,694	UniSTS
CRA_TCAGchr7v2	7	116,343,276 - 116,343,510	UniSTS

REN64009

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,947,567 - 116,947,833	UniSTS	GRCh37
Build 36	7	116,734,803 - 116,735,069	RGD	NCBI36
Celera	7	111,755,748 - 111,756,014	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,313,188 - 111,313,454	UniSTS
CRA_TCAGchr7v2	7	116,343,004 - 116,343,270	UniSTS

REN64010

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,947,315 - 116,947,562	UniSTS	GRCh37
Build 36	7	116,734,551 - 116,734,798	RGD	NCBI36
Celera	7	111,755,496 - 111,755,743	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,312,936 - 111,313,183	UniSTS
CRA_TCAGchr7v2	7	116,342,752 - 116,342,999	UniSTS

REN64011

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,947,058 - 116,947,311	UniSTS	GRCh37
Build 36	7	116,734,294 - 116,734,547	RGD	NCBI36
Celera	7	111,755,239 - 111,755,492	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,312,679 - 111,312,932	UniSTS
CRA_TCAGchr7v2	7	116,342,495 - 116,342,748	UniSTS

REN64012

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,946,775 - 116,946,999	UniSTS	GRCh37
Build 36	7	116,734,011 - 116,734,235	RGD	NCBI36
Celera	7	111,754,956 - 111,755,180	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,312,396 - 111,312,620	UniSTS
CRA_TCAGchr7v2	7	116,342,212 - 116,342,436	UniSTS

REN64013

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,946,526 - 116,946,777	UniSTS	GRCh37
Build 36	7	116,733,762 - 116,734,013	RGD	NCBI36
Celera	7	111,754,707 - 111,754,958	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,312,147 - 111,312,398	UniSTS
CRA_TCAGchr7v2	7	116,341,963 - 116,342,214	UniSTS

REN64014

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,946,294 - 116,946,540	UniSTS	GRCh37
Build 36	7	116,733,530 - 116,733,776	RGD	NCBI36
Celera	7	111,754,475 - 111,754,721	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,311,915 - 111,312,161	UniSTS
CRA_TCAGchr7v2	7	116,341,731 - 116,341,977	UniSTS

REN64015

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,946,032 - 116,946,302	UniSTS	GRCh37
Build 36	7	116,733,268 - 116,733,538	RGD	NCBI36
Celera	7	111,754,213 - 111,754,483	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,311,653 - 111,311,923	UniSTS
CRA_TCAGchr7v2	7	116,341,469 - 116,341,739	UniSTS

REN64016

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,945,789 - 116,946,050	UniSTS	GRCh37
Build 36	7	116,733,025 - 116,733,286	RGD	NCBI36
Celera	7	111,753,970 - 111,754,231	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,311,410 - 111,311,671	UniSTS
CRA_TCAGchr7v2	7	116,341,226 - 116,341,487	UniSTS

REN64017

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,945,564 - 116,945,802	UniSTS	GRCh37
Build 36	7	116,732,800 - 116,733,038	RGD	NCBI36
Celera	7	111,753,745 - 111,753,983	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,311,185 - 111,311,423	UniSTS
CRA_TCAGchr7v2	7	116,341,001 - 116,341,239	UniSTS

REN64018

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,945,270 - 116,945,517	UniSTS	GRCh37
Build 36	7	116,732,506 - 116,732,753	RGD	NCBI36
Celera	7	111,753,451 - 111,753,698	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,310,891 - 111,311,138	UniSTS
CRA_TCAGchr7v2	7	116,340,707 - 116,340,954	UniSTS

REN64019

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,945,033 - 116,945,262	UniSTS	GRCh37
Build 36	7	116,732,269 - 116,732,498	RGD	NCBI36
Celera	7	111,753,214 - 111,753,443	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,310,654 - 111,310,883	UniSTS
CRA_TCAGchr7v2	7	116,340,470 - 116,340,699	UniSTS

REN64020

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,944,806 - 116,945,035	UniSTS	GRCh37
Build 36	7	116,732,042 - 116,732,271	RGD	NCBI36
Celera	7	111,752,987 - 111,753,216	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,310,427 - 111,310,656	UniSTS
CRA_TCAGchr7v2	7	116,340,243 - 116,340,472	UniSTS

REN64021

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,944,178 - 116,944,410	UniSTS	GRCh37
Build 36	7	116,731,414 - 116,731,646	RGD	NCBI36
Celera	7	111,752,362 - 111,752,594	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,309,802 - 111,310,034	UniSTS
CRA_TCAGchr7v2	7	116,339,618 - 116,339,850	UniSTS

REN64022

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,943,926 - 116,944,176	UniSTS	GRCh37
Build 36	7	116,731,162 - 116,731,412	RGD	NCBI36
Celera	7	111,752,110 - 111,752,360	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,309,550 - 111,309,800	UniSTS
CRA_TCAGchr7v2	7	116,339,366 - 116,339,616	UniSTS

REN64023

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,943,689 - 116,943,930	UniSTS	GRCh37
Build 36	7	116,730,925 - 116,731,166	RGD	NCBI36
Celera	7	111,751,873 - 111,752,114	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,309,313 - 111,309,554	UniSTS
CRA_TCAGchr7v2	7	116,339,129 - 116,339,370	UniSTS

REN64024

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,943,435 - 116,943,675	UniSTS	GRCh37
Build 36	7	116,730,671 - 116,730,911	RGD	NCBI36
Celera	7	111,751,619 - 111,751,859	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,309,059 - 111,309,299	UniSTS
CRA_TCAGchr7v2	7	116,338,875 - 116,339,115	UniSTS

REN64025

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,943,214 - 116,943,443	UniSTS	GRCh37
Build 36	7	116,730,450 - 116,730,679	RGD	NCBI36
Celera	7	111,751,398 - 111,751,627	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,308,838 - 111,309,067	UniSTS
CRA_TCAGchr7v2	7	116,338,654 - 116,338,883	UniSTS

REN64026

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,942,964 - 116,943,203	UniSTS	GRCh37
Build 36	7	116,730,200 - 116,730,439	RGD	NCBI36
Celera	7	111,751,148 - 111,751,387	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,308,588 - 111,308,827	UniSTS
CRA_TCAGchr7v2	7	116,338,404 - 116,338,643	UniSTS

REN64027

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,942,732 - 116,942,971	UniSTS	GRCh37
Build 36	7	116,729,968 - 116,730,207	RGD	NCBI36
Celera	7	111,750,916 - 111,751,155	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,308,356 - 111,308,595	UniSTS
CRA_TCAGchr7v2	7	116,338,172 - 116,338,411	UniSTS

REN64028

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,942,495 - 116,942,747	UniSTS	GRCh37
Build 36	7	116,729,731 - 116,729,983	RGD	NCBI36
Celera	7	111,750,679 - 111,750,931	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,308,119 - 111,308,371	UniSTS
CRA_TCAGchr7v2	7	116,337,935 - 116,338,187	UniSTS

REN64029

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,942,247 - 116,942,507	UniSTS	GRCh37
Build 36	7	116,729,483 - 116,729,743	RGD	NCBI36
Celera	7	111,750,431 - 111,750,691	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,307,871 - 111,308,131	UniSTS
CRA_TCAGchr7v2	7	116,337,687 - 116,337,947	UniSTS

REN64030

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,941,833 - 116,942,096	UniSTS	GRCh37
Build 36	7	116,729,069 - 116,729,332	RGD	NCBI36
Celera	7	111,750,017 - 111,750,280	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,307,457 - 111,307,720	UniSTS
CRA_TCAGchr7v2	7	116,337,273 - 116,337,536	UniSTS

REN64031

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,941,570 - 116,941,818	UniSTS	GRCh37
Build 36	7	116,728,806 - 116,729,054	RGD	NCBI36
Celera	7	111,749,754 - 111,750,002	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,307,194 - 111,307,442	UniSTS
CRA_TCAGchr7v2	7	116,337,010 - 116,337,258	UniSTS

REN64032

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,941,357 - 116,941,586	UniSTS	GRCh37
Build 36	7	116,728,593 - 116,728,822	RGD	NCBI36
Celera	7	111,749,541 - 111,749,770	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,306,981 - 111,307,210	UniSTS
CRA_TCAGchr7v2	7	116,336,797 - 116,337,026	UniSTS

REN64033

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,941,106 - 116,941,352	UniSTS	GRCh37
Build 36	7	116,728,342 - 116,728,588	RGD	NCBI36
Celera	7	111,749,290 - 111,749,536	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,306,730 - 111,306,976	UniSTS
CRA_TCAGchr7v2	7	116,336,546 - 116,336,792	UniSTS

REN64034

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,940,878 - 116,941,102	UniSTS	GRCh37
Build 36	7	116,728,114 - 116,728,338	RGD	NCBI36
Celera	7	111,749,061 - 111,749,285	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,306,501 - 111,306,725	UniSTS
CRA_TCAGchr7v2	7	116,336,317 - 116,336,541	UniSTS

REN64035

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,940,529 - 116,940,793	UniSTS	GRCh37
Build 36	7	116,727,765 - 116,728,029	RGD	NCBI36
Celera	7	111,748,712 - 111,748,976	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,306,152 - 111,306,416	UniSTS
CRA_TCAGchr7v2	7	116,335,968 - 116,336,232	UniSTS

REN64036

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,939,760 - 116,940,008	UniSTS	GRCh37
Build 36	7	116,726,996 - 116,727,244	RGD	NCBI36
Celera	7	111,747,943 - 111,748,191	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,305,383 - 111,305,631	UniSTS
CRA_TCAGchr7v2	7	116,335,199 - 116,335,447	UniSTS

REN64037

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,939,369 - 116,939,623	UniSTS	GRCh37
Build 36	7	116,726,605 - 116,726,859	RGD	NCBI36
Celera	7	111,747,552 - 111,747,806	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,304,992 - 111,305,246	UniSTS
CRA_TCAGchr7v2	7	116,334,808 - 116,335,062	UniSTS

REN64038

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,939,033 - 116,939,262	UniSTS	GRCh37
Build 36	7	116,726,269 - 116,726,498	RGD	NCBI36
Celera	7	111,747,216 - 111,747,445	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,304,656 - 111,304,885	UniSTS
CRA_TCAGchr7v2	7	116,334,472 - 116,334,701	UniSTS

REN64039

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,938,817 - 116,939,049	UniSTS	GRCh37
Build 36	7	116,726,053 - 116,726,285	RGD	NCBI36
Celera	7	111,747,000 - 111,747,232	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,304,440 - 111,304,672	UniSTS
CRA_TCAGchr7v2	7	116,334,256 - 116,334,488	UniSTS

REN64040

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,938,564 - 116,938,809	UniSTS	GRCh37
Build 36	7	116,725,800 - 116,726,045	RGD	NCBI36
Celera	7	111,746,747 - 111,746,992	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,304,187 - 111,304,432	UniSTS
CRA_TCAGchr7v2	7	116,334,003 - 116,334,248	UniSTS

REN64041

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,938,354 - 116,938,578	UniSTS	GRCh37
Build 36	7	116,725,590 - 116,725,814	RGD	NCBI36
Celera	7	111,746,537 - 111,746,761	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,303,977 - 111,304,201	UniSTS
CRA_TCAGchr7v2	7	116,333,793 - 116,334,017	UniSTS

REN64042

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,938,074 - 116,938,313	UniSTS	GRCh37
Build 36	7	116,725,310 - 116,725,549	RGD	NCBI36
Celera	7	111,746,257 - 111,746,496	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,303,697 - 111,303,936	UniSTS
CRA_TCAGchr7v2	7	116,333,513 - 116,333,752	UniSTS

REN64043

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,937,820 - 116,938,069	UniSTS	GRCh37
Build 36	7	116,725,056 - 116,725,305	RGD	NCBI36
Celera	7	111,746,003 - 111,746,252	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,303,443 - 111,303,692	UniSTS
CRA_TCAGchr7v2	7	116,333,259 - 116,333,508	UniSTS

REN64044

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,937,576 - 116,937,826	UniSTS	GRCh37
Build 36	7	116,724,812 - 116,725,062	RGD	NCBI36
Celera	7	111,745,759 - 111,746,009	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,303,199 - 111,303,449	UniSTS
CRA_TCAGchr7v2	7	116,333,015 - 116,333,265	UniSTS

REN64045

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,937,357 - 116,937,583	UniSTS	GRCh37
Build 36	7	116,724,593 - 116,724,819	RGD	NCBI36
Celera	7	111,745,540 - 111,745,766	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,302,980 - 111,303,206	UniSTS
CRA_TCAGchr7v2	7	116,332,796 - 116,333,022	UniSTS

REN64046

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,936,985 - 116,937,244	UniSTS	GRCh37
Build 36	7	116,724,221 - 116,724,480	RGD	NCBI36
Celera	7	111,745,168 - 111,745,427	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,302,608 - 111,302,867	UniSTS
CRA_TCAGchr7v2	7	116,332,424 - 116,332,683	UniSTS

REN64047

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,936,737 - 116,936,989	UniSTS	GRCh37
Build 36	7	116,723,973 - 116,724,225	RGD	NCBI36
Celera	7	111,744,920 - 111,745,172	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,302,360 - 111,302,612	UniSTS
CRA_TCAGchr7v2	7	116,332,176 - 116,332,428	UniSTS

REN64048

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,936,508 - 116,936,743	UniSTS	GRCh37
Build 36	7	116,723,744 - 116,723,979	RGD	NCBI36
Celera	7	111,744,691 - 111,744,926	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,302,131 - 111,302,366	UniSTS
CRA_TCAGchr7v2	7	116,331,947 - 116,332,182	UniSTS

REN64049

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,936,265 - 116,936,498	UniSTS	GRCh37
Build 36	7	116,723,501 - 116,723,734	RGD	NCBI36
Celera	7	111,744,448 - 111,744,681	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,301,888 - 111,302,121	UniSTS
CRA_TCAGchr7v2	7	116,331,704 - 116,331,937	UniSTS

REN64050

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,935,998 - 116,936,254	UniSTS	GRCh37
Build 36	7	116,723,234 - 116,723,490	RGD	NCBI36
Celera	7	111,744,181 - 111,744,437	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,301,621 - 111,301,877	UniSTS
CRA_TCAGchr7v2	7	116,331,437 - 116,331,693	UniSTS

REN64051

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,935,768 - 116,936,014	UniSTS	GRCh37
Build 36	7	116,723,004 - 116,723,250	RGD	NCBI36
Celera	7	111,743,951 - 111,744,197	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,301,391 - 111,301,637	UniSTS
CRA_TCAGchr7v2	7	116,331,207 - 116,331,453	UniSTS

REN64052

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,935,504 - 116,935,764	UniSTS	GRCh37
Build 36	7	116,722,740 - 116,723,000	RGD	NCBI36
Celera	7	111,743,687 - 111,743,947	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,301,127 - 111,301,387	UniSTS
CRA_TCAGchr7v2	7	116,330,943 - 116,331,203	UniSTS

REN64053

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,935,243 - 116,935,504	UniSTS	GRCh37
Build 36	7	116,722,479 - 116,722,740	RGD	NCBI36
Celera	7	111,743,426 - 111,743,687	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,300,866 - 111,301,127	UniSTS
CRA_TCAGchr7v2	7	116,330,682 - 116,330,943	UniSTS

REN64054

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,934,992 - 116,935,226	UniSTS	GRCh37
Build 36	7	116,722,228 - 116,722,462	RGD	NCBI36
Celera	7	111,743,175 - 111,743,409	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,300,615 - 111,300,849	UniSTS
CRA_TCAGchr7v2	7	116,330,431 - 116,330,665	UniSTS

REN64055

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,934,602 - 116,934,833	UniSTS	GRCh37
Build 36	7	116,721,838 - 116,722,069	RGD	NCBI36
Celera	7	111,742,786 - 111,743,016	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,300,226 - 111,300,456	UniSTS
CRA_TCAGchr7v2	7	116,330,041 - 116,330,272	UniSTS

REN64056

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,934,264 - 116,934,533	UniSTS	GRCh37
Build 36	7	116,721,500 - 116,721,769	RGD	NCBI36
Celera	7	111,742,448 - 111,742,717	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,299,888 - 111,300,157	UniSTS
CRA_TCAGchr7v2	7	116,329,703 - 116,329,972	UniSTS

REN64057

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,934,030 - 116,934,279	UniSTS	GRCh37
Build 36	7	116,721,266 - 116,721,515	RGD	NCBI36
Celera	7	111,742,214 - 111,742,463	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,299,654 - 111,299,903	UniSTS
CRA_TCAGchr7v2	7	116,329,469 - 116,329,718	UniSTS

REN64058

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,933,742 - 116,933,986	UniSTS	GRCh37
Build 36	7	116,720,978 - 116,721,222	RGD	NCBI36
Celera	7	111,741,926 - 111,742,170	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,299,366 - 111,299,610	UniSTS
CRA_TCAGchr7v2	7	116,329,181 - 116,329,425	UniSTS

REN64059

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,933,507 - 116,933,747	UniSTS	GRCh37
Build 36	7	116,720,743 - 116,720,983	RGD	NCBI36
Celera	7	111,741,691 - 111,741,931	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,299,131 - 111,299,371	UniSTS
CRA_TCAGchr7v2	7	116,328,946 - 116,329,186	UniSTS

REN64060

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,933,226 - 116,933,482	UniSTS	GRCh37
Build 36	7	116,720,462 - 116,720,718	RGD	NCBI36
Celera	7	111,741,410 - 111,741,666	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,298,850 - 111,299,106	UniSTS
CRA_TCAGchr7v2	7	116,328,665 - 116,328,921	UniSTS

REN64061

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,932,964 - 116,933,232	UniSTS	GRCh37
Build 36	7	116,720,200 - 116,720,468	RGD	NCBI36
Celera	7	111,741,148 - 111,741,416	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,298,588 - 111,298,856	UniSTS
CRA_TCAGchr7v2	7	116,328,403 - 116,328,671	UniSTS

REN64062

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,932,731 - 116,932,955	UniSTS	GRCh37
Build 36	7	116,719,967 - 116,720,191	RGD	NCBI36
Celera	7	111,740,915 - 111,741,139	RGD
Cytogenetic Map	7	q31.2	UniSTS
CRA_TCAGchr7v2	7	116,328,170 - 116,328,394	UniSTS

REN64063

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,932,497 - 116,932,727	UniSTS	GRCh37
Build 36	7	116,719,733 - 116,719,963	RGD	NCBI36
Celera	7	111,740,681 - 111,740,911	RGD
Cytogenetic Map	7	q31.2	UniSTS
CRA_TCAGchr7v2	7	116,327,936 - 116,328,166	UniSTS

REN64064

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,932,250 - 116,932,515	UniSTS	GRCh37
Build 36	7	116,719,486 - 116,719,751	RGD	NCBI36
Celera	7	111,740,434 - 111,740,699	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,298,074 - 111,298,339	UniSTS
CRA_TCAGchr7v2	7	116,327,689 - 116,327,954	UniSTS

REN64065

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,932,019 - 116,932,268	UniSTS	GRCh37
Build 36	7	116,719,255 - 116,719,504	RGD	NCBI36
Celera	7	111,740,203 - 111,740,452	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,297,843 - 111,298,092	UniSTS
CRA_TCAGchr7v2	7	116,327,458 - 116,327,707	UniSTS

REN64066

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,931,778 - 116,932,038	UniSTS	GRCh37
Build 36	7	116,719,014 - 116,719,274	RGD	NCBI36
Celera	7	111,739,962 - 111,740,222	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,297,602 - 111,297,862	UniSTS
CRA_TCAGchr7v2	7	116,327,217 - 116,327,477	UniSTS

REN64067

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,931,550 - 116,931,794	UniSTS	GRCh37
Build 36	7	116,718,786 - 116,719,030	RGD	NCBI36
Celera	7	111,739,734 - 111,739,978	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,297,374 - 111,297,618	UniSTS
CRA_TCAGchr7v2	7	116,326,989 - 116,327,233	UniSTS

REN64068

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,931,332 - 116,931,562	UniSTS	GRCh37
Build 36	7	116,718,568 - 116,718,798	RGD	NCBI36
Celera	7	111,739,516 - 111,739,746	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,297,156 - 111,297,386	UniSTS
CRA_TCAGchr7v2	7	116,326,771 - 116,327,001	UniSTS

REN64069

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,931,094 - 116,931,331	UniSTS	GRCh37
Build 36	7	116,718,330 - 116,718,567	RGD	NCBI36
Celera	7	111,739,278 - 111,739,515	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,296,918 - 111,297,155	UniSTS
CRA_TCAGchr7v2	7	116,326,533 - 116,326,770	UniSTS

REN64070

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,930,847 - 116,931,099	UniSTS	GRCh37
Build 36	7	116,718,083 - 116,718,335	RGD	NCBI36
Celera	7	111,739,031 - 111,739,283	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,296,671 - 111,296,923	UniSTS
CRA_TCAGchr7v2	7	116,326,286 - 116,326,538	UniSTS

REN64071

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,930,629 - 116,930,855	UniSTS	GRCh37
Build 36	7	116,717,865 - 116,718,091	RGD	NCBI36
Celera	7	111,738,813 - 111,739,039	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,296,453 - 111,296,679	UniSTS
CRA_TCAGchr7v2	7	116,326,068 - 116,326,294	UniSTS

REN64072

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,930,367 - 116,930,602	UniSTS	GRCh37
Build 36	7	116,717,603 - 116,717,838	RGD	NCBI36
Celera	7	111,738,551 - 111,738,786	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,296,191 - 111,296,426	UniSTS
CRA_TCAGchr7v2	7	116,325,806 - 116,326,041	UniSTS

REN64073

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,930,140 - 116,930,373	UniSTS	GRCh37
Build 36	7	116,717,376 - 116,717,609	RGD	NCBI36
Celera	7	111,738,324 - 111,738,557	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,295,964 - 111,296,197	UniSTS
CRA_TCAGchr7v2	7	116,325,579 - 116,325,812	UniSTS

REN64074

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,929,898 - 116,930,134	UniSTS	GRCh37
Build 36	7	116,717,134 - 116,717,370	RGD	NCBI36
Celera	7	111,738,082 - 111,738,318	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,295,722 - 111,295,958	UniSTS
CRA_TCAGchr7v2	7	116,325,337 - 116,325,573	UniSTS

REN64075

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,929,690 - 116,929,914	UniSTS	GRCh37
Build 36	7	116,716,926 - 116,717,150	RGD	NCBI36
Celera	7	111,737,874 - 111,738,098	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,295,514 - 111,295,738	UniSTS
CRA_TCAGchr7v2	7	116,325,129 - 116,325,353	UniSTS

REN64076

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,929,436 - 116,929,660	UniSTS	GRCh37
Build 36	7	116,716,672 - 116,716,896	RGD	NCBI36
Celera	7	111,737,620 - 111,737,844	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,295,260 - 111,295,484	UniSTS
CRA_TCAGchr7v2	7	116,324,875 - 116,325,099	UniSTS

REN64077

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,929,209 - 116,929,447	UniSTS	GRCh37
Build 36	7	116,716,445 - 116,716,683	RGD	NCBI36
Celera	7	111,737,393 - 111,737,631	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,295,033 - 111,295,271	UniSTS
CRA_TCAGchr7v2	7	116,324,648 - 116,324,886	UniSTS

REN64078

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,928,826 - 116,929,071	UniSTS	GRCh37
Build 36	7	116,716,062 - 116,716,307	RGD	NCBI36
Celera	7	111,737,010 - 111,737,255	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,294,650 - 111,294,895	UniSTS
CRA_TCAGchr7v2	7	116,324,265 - 116,324,510	UniSTS

REN64079

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,928,590 - 116,928,826	UniSTS	GRCh37
Build 36	7	116,715,826 - 116,716,062	RGD	NCBI36
Celera	7	111,736,774 - 111,737,010	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,294,414 - 111,294,650	UniSTS
CRA_TCAGchr7v2	7	116,324,029 - 116,324,265	UniSTS

REN64080

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,928,264 - 116,928,490	UniSTS	GRCh37
Build 36	7	116,715,500 - 116,715,726	RGD	NCBI36
Celera	7	111,736,448 - 111,736,674	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,294,088 - 111,294,314	UniSTS
CRA_TCAGchr7v2	7	116,323,703 - 116,323,929	UniSTS

REN64081

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,928,028 - 116,928,282	UniSTS	GRCh37
Build 36	7	116,715,264 - 116,715,518	RGD	NCBI36
Celera	7	111,736,212 - 111,736,466	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,293,852 - 111,294,106	UniSTS
CRA_TCAGchr7v2	7	116,323,467 - 116,323,721	UniSTS

REN64082

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,927,418 - 116,927,642	UniSTS	GRCh37
Build 36	7	116,714,654 - 116,714,878	RGD	NCBI36
Celera	7	111,735,602 - 111,735,826	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,293,242 - 111,293,466	UniSTS
CRA_TCAGchr7v2	7	116,322,857 - 116,323,081	UniSTS

REN64083

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,926,785 - 116,927,015	UniSTS	GRCh37
Build 36	7	116,714,021 - 116,714,251	RGD	NCBI36
Celera	7	111,734,966 - 111,735,199	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,292,589 - 111,292,839	UniSTS
CRA_TCAGchr7v2	7	116,322,224 - 116,322,454	UniSTS

REN64084

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,926,518 - 116,926,764	UniSTS	GRCh37
Build 36	7	116,713,754 - 116,714,000	RGD	NCBI36
Celera	7	111,734,699 - 111,734,945	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,292,322 - 111,292,568	UniSTS
CRA_TCAGchr7v2	7	116,321,957 - 116,322,203	UniSTS

REN64085

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,926,272 - 116,926,531	UniSTS	GRCh37
Build 36	7	116,713,508 - 116,713,767	RGD	NCBI36
Celera	7	111,734,453 - 111,734,712	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,292,076 - 111,292,335	UniSTS
CRA_TCAGchr7v2	7	116,321,711 - 116,321,970	UniSTS

REN64086

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,926,043 - 116,926,283	UniSTS	GRCh37
Build 36	7	116,713,279 - 116,713,519	RGD	NCBI36
Celera	7	111,734,224 - 111,734,464	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,291,847 - 111,292,087	UniSTS
CRA_TCAGchr7v2	7	116,321,482 - 116,321,722	UniSTS

REN64087

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,925,823 - 116,926,061	UniSTS	GRCh37
Build 36	7	116,713,059 - 116,713,297	RGD	NCBI36
Celera	7	111,734,004 - 111,734,242	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,291,627 - 111,291,865	UniSTS
CRA_TCAGchr7v2	7	116,321,262 - 116,321,500	UniSTS

REN64088

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,925,562 - 116,925,806	UniSTS	GRCh37
Build 36	7	116,712,798 - 116,713,042	RGD	NCBI36
Celera	7	111,733,743 - 111,733,987	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,291,366 - 111,291,610	UniSTS
CRA_TCAGchr7v2	7	116,321,001 - 116,321,245	UniSTS

REN64089

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,925,309 - 116,925,562	UniSTS	GRCh37
Build 36	7	116,712,545 - 116,712,798	RGD	NCBI36
Celera	7	111,733,490 - 111,733,743	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,291,113 - 111,291,366	UniSTS
CRA_TCAGchr7v2	7	116,320,748 - 116,321,001	UniSTS

REN64090

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,925,069 - 116,925,296	UniSTS	GRCh37
Build 36	7	116,712,305 - 116,712,532	RGD	NCBI36
Celera	7	111,733,250 - 111,733,477	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,290,873 - 111,291,100	UniSTS
CRA_TCAGchr7v2	7	116,320,508 - 116,320,735	UniSTS

REN64091

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,924,818 - 116,925,045	UniSTS	GRCh37
Build 36	7	116,712,054 - 116,712,281	RGD	NCBI36
Celera	7	111,732,999 - 111,733,226	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,290,622 - 111,290,849	UniSTS
CRA_TCAGchr7v2	7	116,320,257 - 116,320,484	UniSTS

REN64092

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,924,586 - 116,924,836	UniSTS	GRCh37
Build 36	7	116,711,822 - 116,712,072	RGD	NCBI36
Celera	7	111,732,767 - 111,733,017	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,290,390 - 111,290,640	UniSTS
CRA_TCAGchr7v2	7	116,320,025 - 116,320,275	UniSTS

REN64093

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,924,349 - 116,924,585	UniSTS	GRCh37
Build 36	7	116,711,585 - 116,711,821	RGD	NCBI36
Celera	7	111,732,530 - 111,732,766	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,290,153 - 111,290,389	UniSTS
CRA_TCAGchr7v2	7	116,319,788 - 116,320,024	UniSTS

REN64094

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,924,081 - 116,924,332	UniSTS	GRCh37
Build 36	7	116,711,317 - 116,711,568	RGD	NCBI36
Celera	7	111,732,262 - 111,732,513	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,289,885 - 111,290,136	UniSTS
CRA_TCAGchr7v2	7	116,319,520 - 116,319,771	UniSTS

REN64095

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,923,852 - 116,924,078	UniSTS	GRCh37
Build 36	7	116,711,088 - 116,711,314	RGD	NCBI36
Celera	7	111,732,033 - 111,732,259	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,289,656 - 111,289,882	UniSTS
CRA_TCAGchr7v2	7	116,319,291 - 116,319,517	UniSTS

REN64096

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,923,592 - 116,923,826	UniSTS	GRCh37
Build 36	7	116,710,828 - 116,711,062	RGD	NCBI36
Celera	7	111,731,773 - 111,732,007	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,289,396 - 111,289,630	UniSTS
CRA_TCAGchr7v2	7	116,319,031 - 116,319,265	UniSTS

REN64097

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,923,327 - 116,923,587	UniSTS	GRCh37
Build 36	7	116,710,563 - 116,710,823	RGD	NCBI36
Celera	7	111,731,508 - 111,731,768	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,289,131 - 111,289,391	UniSTS
CRA_TCAGchr7v2	7	116,318,766 - 116,319,026	UniSTS

REN64098

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,923,100 - 116,923,338	UniSTS	GRCh37
Build 36	7	116,710,336 - 116,710,574	RGD	NCBI36
Celera	7	111,731,281 - 111,731,519	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,288,904 - 111,289,142	UniSTS
CRA_TCAGchr7v2	7	116,318,539 - 116,318,777	UniSTS

REN64099

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,922,859 - 116,923,087	UniSTS	GRCh37
Build 36	7	116,710,095 - 116,710,323	RGD	NCBI36
Celera	7	111,731,040 - 111,731,268	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,288,663 - 111,288,891	UniSTS
CRA_TCAGchr7v2	7	116,318,298 - 116,318,526	UniSTS

REN64100

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,922,592 - 116,922,832	UniSTS	GRCh37
Build 36	7	116,709,828 - 116,710,068	RGD	NCBI36
Celera	7	111,730,773 - 111,731,013	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,288,396 - 111,288,636	UniSTS
CRA_TCAGchr7v2	7	116,318,031 - 116,318,271	UniSTS

REN64101

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,922,348 - 116,922,588	UniSTS	GRCh37
Build 36	7	116,709,584 - 116,709,824	RGD	NCBI36
Celera	7	111,730,526 - 111,730,769	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,288,149 - 111,288,392	UniSTS
CRA_TCAGchr7v2	7	116,317,784 - 116,318,027	UniSTS

REN64102

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,922,107 - 116,922,331	UniSTS	GRCh37
Build 36	7	116,709,343 - 116,709,567	RGD	NCBI36
Celera	7	111,730,285 - 111,730,509	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,287,908 - 111,288,132	UniSTS
CRA_TCAGchr7v2	7	116,317,543 - 116,317,767	UniSTS

REN64103

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,921,869 - 116,922,110	UniSTS	GRCh37
Build 36	7	116,709,105 - 116,709,346	RGD	NCBI36
Celera	7	111,730,047 - 111,730,288	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,287,670 - 111,287,911	UniSTS
CRA_TCAGchr7v2	7	116,317,305 - 116,317,546	UniSTS

REN64104

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,921,627 - 116,921,857	UniSTS	GRCh37
Build 36	7	116,708,863 - 116,709,093	RGD	NCBI36
Celera	7	111,729,805 - 111,730,035	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,287,428 - 111,287,658	UniSTS
CRA_TCAGchr7v2	7	116,317,063 - 116,317,293	UniSTS

REN64105

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,921,358 - 116,921,621	UniSTS	GRCh37
Build 36	7	116,708,594 - 116,708,857	RGD	NCBI36
Celera	7	111,729,536 - 111,729,799	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,287,159 - 111,287,422	UniSTS
CRA_TCAGchr7v2	7	116,316,794 - 116,317,057	UniSTS

REN64106

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,921,137 - 116,921,375	UniSTS	GRCh37
Build 36	7	116,708,373 - 116,708,611	RGD	NCBI36
Celera	7	111,729,315 - 111,729,553	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,286,938 - 111,287,176	UniSTS
CRA_TCAGchr7v2	7	116,316,573 - 116,316,811	UniSTS

REN64107

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,920,918 - 116,921,156	UniSTS	GRCh37
Build 36	7	116,708,154 - 116,708,392	RGD	NCBI36
Celera	7	111,729,096 - 111,729,334	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,286,719 - 111,286,957	UniSTS
CRA_TCAGchr7v2	7	116,316,354 - 116,316,592	UniSTS

REN64108

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,920,667 - 116,920,915	UniSTS	GRCh37
Build 36	7	116,707,903 - 116,708,151	RGD	NCBI36
Celera	7	111,728,845 - 111,729,093	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,286,468 - 111,286,716	UniSTS
CRA_TCAGchr7v2	7	116,316,103 - 116,316,351	UniSTS

REN64109

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,920,421 - 116,920,664	UniSTS	GRCh37
Build 36	7	116,707,657 - 116,707,900	RGD	NCBI36
Celera	7	111,728,599 - 111,728,842	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,286,222 - 111,286,465	UniSTS
CRA_TCAGchr7v2	7	116,315,857 - 116,316,100	UniSTS

REN64110

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,920,179 - 116,920,409	UniSTS	GRCh37
Build 36	7	116,707,415 - 116,707,645	RGD	NCBI36
Celera	7	111,728,357 - 111,728,587	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,285,980 - 111,286,210	UniSTS
CRA_TCAGchr7v2	7	116,315,615 - 116,315,845	UniSTS

REN64111

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,919,959 - 116,920,198	UniSTS	GRCh37
Build 36	7	116,707,195 - 116,707,434	RGD	NCBI36
Celera	7	111,728,137 - 111,728,376	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,285,760 - 111,285,999	UniSTS
CRA_TCAGchr7v2	7	116,315,395 - 116,315,634	UniSTS

REN64112

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,919,689 - 116,919,961	UniSTS	GRCh37
Build 36	7	116,706,925 - 116,707,197	RGD	NCBI36
Celera	7	111,727,867 - 111,728,139	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,285,490 - 111,285,762	UniSTS
CRA_TCAGchr7v2	7	116,315,125 - 116,315,397	UniSTS

REN64113

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,919,467 - 116,919,707	UniSTS	GRCh37
Build 36	7	116,706,703 - 116,706,943	RGD	NCBI36
Celera	7	111,727,645 - 111,727,885	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,285,268 - 111,285,508	UniSTS
CRA_TCAGchr7v2	7	116,314,903 - 116,315,143	UniSTS

REN64114

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,919,257 - 116,919,481	UniSTS	GRCh37
Build 36	7	116,706,493 - 116,706,717	RGD	NCBI36
Celera	7	111,727,435 - 111,727,659	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,285,058 - 111,285,282	UniSTS
CRA_TCAGchr7v2	7	116,314,693 - 116,314,917	UniSTS

REN64115

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,918,992 - 116,919,226	UniSTS	GRCh37
Build 36	7	116,706,228 - 116,706,462	RGD	NCBI36
Celera	7	111,727,170 - 111,727,404	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,284,793 - 111,285,027	UniSTS
CRA_TCAGchr7v2	7	116,314,428 - 116,314,662	UniSTS

REN64116

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,918,777 - 116,919,010	UniSTS	GRCh37
Build 36	7	116,706,013 - 116,706,246	RGD	NCBI36
Celera	7	111,726,955 - 111,727,188	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,284,578 - 111,284,811	UniSTS
CRA_TCAGchr7v2	7	116,314,213 - 116,314,446	UniSTS

REN64117

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,918,533 - 116,918,758	UniSTS	GRCh37
Build 36	7	116,705,769 - 116,705,994	RGD	NCBI36
Celera	7	111,726,711 - 111,726,936	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,284,334 - 111,284,559	UniSTS
CRA_TCAGchr7v2	7	116,313,969 - 116,314,194	UniSTS

REN64118

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,918,301 - 116,918,525	UniSTS	GRCh37
Build 36	7	116,705,537 - 116,705,761	RGD	NCBI36
Celera	7	111,726,479 - 111,726,703	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,284,102 - 111,284,326	UniSTS
CRA_TCAGchr7v2	7	116,313,737 - 116,313,961	UniSTS

REN64119

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,918,025 - 116,918,282	UniSTS	GRCh37
Build 36	7	116,705,261 - 116,705,518	RGD	NCBI36
Celera	7	111,726,203 - 111,726,460	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,283,826 - 111,284,083	UniSTS
CRA_TCAGchr7v2	7	116,313,461 - 116,313,718	UniSTS

REN64120

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,798 - 116,918,037	UniSTS	GRCh37
Build 36	7	116,705,034 - 116,705,273	RGD	NCBI36
Celera	7	111,725,976 - 111,726,215	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,283,599 - 111,283,838	UniSTS
CRA_TCAGchr7v2	7	116,313,234 - 116,313,473	UniSTS

REN64121

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,553 - 116,917,797	UniSTS	GRCh37
Build 36	7	116,704,789 - 116,705,033	RGD	NCBI36
Celera	7	111,725,731 - 111,725,975	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,283,354 - 111,283,598	UniSTS
CRA_TCAGchr7v2	7	116,312,989 - 116,313,233	UniSTS

REN64122

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,337 - 116,917,562	UniSTS	GRCh37
Build 36	7	116,704,573 - 116,704,798	RGD	NCBI36
Celera	7	111,725,515 - 111,725,740	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,283,138 - 111,283,363	UniSTS
CRA_TCAGchr7v2	7	116,312,773 - 116,312,998	UniSTS

REN64123

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,069 - 116,917,293	UniSTS	GRCh37
Build 36	7	116,704,305 - 116,704,529	RGD	NCBI36
Celera	7	111,725,246 - 111,725,471	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,282,869 - 111,283,094	UniSTS
CRA_TCAGchr7v2	7	116,312,504 - 116,312,729	UniSTS

REN64124

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,916,832 - 116,917,056	UniSTS	GRCh37
Build 36	7	116,704,068 - 116,704,292	RGD	NCBI36
Celera	7	111,725,009 - 111,725,233	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,282,632 - 111,282,856	UniSTS
CRA_TCAGchr7v2	7	116,312,267 - 116,312,491	UniSTS

REN64125

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,916,583 - 116,916,811	UniSTS	GRCh37
Build 36	7	116,703,819 - 116,704,047	RGD	NCBI36
Celera	7	111,724,760 - 111,724,988	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,282,383 - 111,282,611	UniSTS
CRA_TCAGchr7v2	7	116,312,018 - 116,312,246	UniSTS

REN64126

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,916,313 - 116,916,566	UniSTS	GRCh37
Build 36	7	116,703,549 - 116,703,802	RGD	NCBI36
Celera	7	111,724,490 - 111,724,743	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,282,113 - 111,282,366	UniSTS
CRA_TCAGchr7v2	7	116,311,748 - 116,312,001	UniSTS

stSG598541

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,076 - 116,918,239	UniSTS	GRCh37
Build 36	7	116,704,312 - 116,705,475	RGD	NCBI36
Celera	7	111,725,253 - 111,726,417	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,282,876 - 111,284,040	UniSTS
CRA_TCAGchr7v2	7	116,312,511 - 116,313,675	UniSTS

stSG598542

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,918,220 - 116,919,487	UniSTS	GRCh37
Build 36	7	116,705,456 - 116,706,723	RGD	NCBI36
Celera	7	111,726,398 - 111,727,665	RGD
HuRef	7	111,284,021 - 111,285,288	UniSTS
CRA_TCAGchr7v2	7	116,313,656 - 116,314,923	UniSTS

stSG598543

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,919,547 - 116,920,646	UniSTS	GRCh37
Build 36	7	116,706,783 - 116,707,882	RGD	NCBI36
Celera	7	111,727,725 - 111,728,824	RGD
HuRef	7	111,285,348 - 111,286,447	UniSTS
CRA_TCAGchr7v2	7	116,314,983 - 116,316,082	UniSTS

stSG598544

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,920,627 - 116,922,066	UniSTS	GRCh37
Build 36	7	116,707,863 - 116,709,302	RGD	NCBI36
Celera	7	111,728,805 - 111,730,244	RGD
HuRef	7	111,286,428 - 111,287,867	UniSTS
CRA_TCAGchr7v2	7	116,316,063 - 116,317,502	UniSTS

stSG598545

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,922,047 - 116,923,484	UniSTS	GRCh37
Build 36	7	116,709,283 - 116,710,720	RGD	NCBI36
Celera	7	111,730,225 - 111,731,665	RGD
HuRef	7	111,287,848 - 111,289,288	UniSTS
CRA_TCAGchr7v2	7	116,317,483 - 116,318,923	UniSTS

stSG598546

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,923,465 - 116,924,600	UniSTS	GRCh37
Build 36	7	116,710,701 - 116,711,836	RGD	NCBI36
Celera	7	111,731,646 - 111,732,781	RGD
HuRef	7	111,289,269 - 111,290,404	UniSTS
CRA_TCAGchr7v2	7	116,318,904 - 116,320,039	UniSTS

stSG598547

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,924,581 - 116,925,956	UniSTS	GRCh37
Build 36	7	116,711,817 - 116,713,192	RGD	NCBI36
Celera	7	111,732,762 - 111,734,137	RGD
HuRef	7	111,290,385 - 111,291,760	UniSTS
CRA_TCAGchr7v2	7	116,320,020 - 116,321,395	UniSTS

stSG598548

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,925,937 - 116,926,983	UniSTS	GRCh37
Build 36	7	116,713,173 - 116,714,219	RGD	NCBI36
Celera	7	111,734,118 - 111,735,167	RGD
HuRef	7	111,291,741 - 111,292,807	UniSTS
CRA_TCAGchr7v2	7	116,321,376 - 116,322,422	UniSTS

stSG598549

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,927,050 - 116,928,167	UniSTS	GRCh37
Build 36	7	116,714,286 - 116,715,403	RGD	NCBI36
Celera	7	111,735,234 - 111,736,351	RGD
HuRef	7	111,292,874 - 111,293,991	UniSTS
CRA_TCAGchr7v2	7	116,322,489 - 116,323,606	UniSTS

stSG598550

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,928,148 - 116,929,463	UniSTS	GRCh37
Build 36	7	116,715,384 - 116,716,699	RGD	NCBI36
Celera	7	111,736,332 - 111,737,647	RGD
HuRef	7	111,293,972 - 111,295,287	UniSTS
CRA_TCAGchr7v2	7	116,323,587 - 116,324,902	UniSTS

stSG598551

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,929,444 - 116,930,755	UniSTS	GRCh37
Build 36	7	116,716,680 - 116,717,991	RGD	NCBI36
Celera	7	111,737,628 - 111,738,939	RGD
HuRef	7	111,295,268 - 111,296,579	UniSTS
CRA_TCAGchr7v2	7	116,324,883 - 116,326,194	UniSTS

stSG598552

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,930,736 - 116,932,191	UniSTS	GRCh37
Build 36	7	116,717,972 - 116,719,427	RGD	NCBI36
Celera	7	111,738,920 - 111,740,375	RGD
HuRef	7	111,296,560 - 111,298,015	UniSTS
CRA_TCAGchr7v2	7	116,326,175 - 116,327,630	UniSTS

stSG598553

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,932,254 - 116,933,607	UniSTS	GRCh37
Build 36	7	116,719,490 - 116,720,843	RGD	NCBI36
Celera	7	111,740,438 - 111,741,791	RGD
HuRef	7	111,298,078 - 111,299,231	UniSTS
CRA_TCAGchr7v2	7	116,327,693 - 116,329,046	UniSTS

stSG598554

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,933,588 - 116,934,861	UniSTS	GRCh37
Build 36	7	116,720,824 - 116,722,097	RGD	NCBI36
Celera	7	111,741,772 - 111,743,044	RGD
HuRef	7	111,299,212 - 111,300,484	UniSTS
CRA_TCAGchr7v2	7	116,329,027 - 116,330,300	UniSTS

stSG598555

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,934,842 - 116,935,846	UniSTS	GRCh37
Build 36	7	116,722,078 - 116,723,082	RGD	NCBI36
Celera	7	111,743,025 - 111,744,029	RGD
HuRef	7	111,300,465 - 111,301,469	UniSTS
CRA_TCAGchr7v2	7	116,330,281 - 116,331,285	UniSTS

stSG598556

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,935,831 - 116,936,030	UniSTS	GRCh37
Build 36	7	116,723,067 - 116,723,266	RGD	NCBI36
Celera	7	111,744,014 - 111,744,213	RGD
HuRef	7	111,301,454 - 111,301,653	UniSTS
CRA_TCAGchr7v2	7	116,331,270 - 116,331,469	UniSTS

stSG598557

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,936,130 - 116,937,207	UniSTS	GRCh37
Build 36	7	116,723,366 - 116,724,443	RGD	NCBI36
Celera	7	111,744,313 - 111,745,390	RGD
HuRef	7	111,301,753 - 111,302,830	UniSTS
CRA_TCAGchr7v2	7	116,331,569 - 116,332,646	UniSTS

stSG598558

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,937,207 - 116,938,383	UniSTS	GRCh37
Build 36	7	116,724,443 - 116,725,619	RGD	NCBI36
Celera	7	111,745,390 - 111,746,566	RGD
HuRef	7	111,302,830 - 111,304,006	UniSTS
CRA_TCAGchr7v2	7	116,332,646 - 116,333,822	UniSTS

stSG598559

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,938,372 - 116,939,395	UniSTS	GRCh37
Build 36	7	116,725,608 - 116,726,631	RGD	NCBI36
Celera	7	111,746,555 - 111,747,578	RGD
HuRef	7	111,303,995 - 111,305,018	UniSTS
CRA_TCAGchr7v2	7	116,333,811 - 116,334,834	UniSTS

stSG598560

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,939,141 - 116,940,182	UniSTS	GRCh37
Build 36	7	116,726,377 - 116,727,418	RGD	NCBI36
Celera	7	111,747,324 - 111,748,365	RGD
HuRef	7	111,304,764 - 111,305,805	UniSTS
CRA_TCAGchr7v2	7	116,334,580 - 116,335,621	UniSTS

stSG598561

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,940,163 - 116,941,229	UniSTS	GRCh37
Build 36	7	116,727,399 - 116,728,465	RGD	NCBI36
Celera	7	111,748,346 - 111,749,413	RGD
HuRef	7	111,305,786 - 111,306,853	UniSTS
CRA_TCAGchr7v2	7	116,335,602 - 116,336,669	UniSTS

stSG598562

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,941,213 - 116,942,228	UniSTS	GRCh37
Build 36	7	116,728,449 - 116,729,464	RGD	NCBI36
Celera	7	111,749,397 - 111,750,412	RGD
HuRef	7	111,306,837 - 111,307,852	UniSTS
CRA_TCAGchr7v2	7	116,336,653 - 116,337,668	UniSTS

stSG598563

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,942,210 - 116,943,553	UniSTS	GRCh37
Build 36	7	116,729,446 - 116,730,789	RGD	NCBI36
Celera	7	111,750,394 - 111,751,737	RGD
HuRef	7	111,307,834 - 111,309,177	UniSTS
CRA_TCAGchr7v2	7	116,337,650 - 116,338,993	UniSTS

stSG598564

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,943,534 - 116,944,958	UniSTS	GRCh37
Build 36	7	116,730,770 - 116,732,194	RGD	NCBI36
Celera	7	111,751,718 - 111,753,139	RGD
HuRef	7	111,309,158 - 111,310,579	UniSTS
CRA_TCAGchr7v2	7	116,338,974 - 116,340,395	UniSTS

stSG598565

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,945,046 - 116,946,398	UniSTS	GRCh37
Build 36	7	116,732,282 - 116,733,634	RGD	NCBI36
Celera	7	111,753,227 - 111,754,579	RGD
HuRef	7	111,310,667 - 111,312,019	UniSTS
CRA_TCAGchr7v2	7	116,340,483 - 116,341,835	UniSTS

stSG598566

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,946,378 - 116,946,557	UniSTS	GRCh37
Build 36	7	116,733,614 - 116,733,793	RGD	NCBI36
Celera	7	111,754,559 - 111,754,738	RGD
HuRef	7	111,311,999 - 111,312,178	UniSTS
CRA_TCAGchr7v2	7	116,341,815 - 116,341,994	UniSTS

stSG598567

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,946,562 - 116,947,563	UniSTS	GRCh37
Build 36	7	116,733,798 - 116,734,799	RGD	NCBI36
Celera	7	111,754,743 - 111,755,744	RGD
HuRef	7	111,312,183 - 111,313,184	UniSTS
CRA_TCAGchr7v2	7	116,341,999 - 116,343,000	UniSTS

stSG598568

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,947,554 - 116,948,760	UniSTS	GRCh37
Build 36	7	116,734,790 - 116,735,996	RGD	NCBI36
Celera	7	111,755,735 - 111,756,941	RGD
HuRef	7	111,313,175 - 111,314,381	UniSTS
CRA_TCAGchr7v2	7	116,342,991 - 116,344,197	UniSTS

stSG598569

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,948,749 - 116,949,765	UniSTS	GRCh37
Build 36	7	116,735,985 - 116,737,001	RGD	NCBI36
Celera	7	111,756,930 - 111,757,946	RGD
HuRef	7	111,314,370 - 111,315,386	UniSTS
CRA_TCAGchr7v2	7	116,344,186 - 116,345,202	UniSTS

stSG598570

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,949,746 - 116,950,938	UniSTS	GRCh37
Build 36	7	116,736,982 - 116,738,174	RGD	NCBI36
Celera	7	111,757,927 - 111,759,119	RGD
HuRef	7	111,315,367 - 111,316,559	UniSTS
CRA_TCAGchr7v2	7	116,345,183 - 116,346,375	UniSTS

stSG598571

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,950,919 - 116,951,934	UniSTS	GRCh37
Build 36	7	116,738,155 - 116,739,170	RGD	NCBI36
Celera	7	111,759,100 - 111,760,115	RGD
HuRef	7	111,316,540 - 111,317,555	UniSTS
CRA_TCAGchr7v2	7	116,346,356 - 116,347,371	UniSTS

stSG598572

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,951,915 - 116,953,268	UniSTS	GRCh37
Build 36	7	116,739,151 - 116,740,504	RGD	NCBI36
Celera	7	111,760,096 - 111,761,449	RGD
HuRef	7	111,317,536 - 111,318,889	UniSTS
CRA_TCAGchr7v2	7	116,347,352 - 116,348,705	UniSTS

stSG598573

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,953,249 - 116,954,639	UniSTS	GRCh37
Build 36	7	116,740,485 - 116,741,875	RGD	NCBI36
Celera	7	111,761,430 - 111,762,820	RGD
HuRef	7	111,318,870 - 111,320,260	UniSTS
CRA_TCAGchr7v2	7	116,348,686 - 116,350,076	UniSTS

stSG598574

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,954,637 - 116,955,985	UniSTS	GRCh37
Build 36	7	116,741,873 - 116,743,221	RGD	NCBI36
Celera	7	111,762,818 - 111,764,166	RGD
HuRef	7	111,320,258 - 111,321,606	UniSTS
CRA_TCAGchr7v2	7	116,350,074 - 116,351,422	UniSTS

stSG598575

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,955,966 - 116,957,337	UniSTS	GRCh37
Build 36	7	116,743,202 - 116,744,573	RGD	NCBI36
Celera	7	111,764,147 - 111,765,518	RGD
HuRef	7	111,321,587 - 111,322,958	UniSTS
CRA_TCAGchr7v2	7	116,351,403 - 116,352,774	UniSTS

stSG598576

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,957,318 - 116,958,395	UniSTS	GRCh37
Build 36	7	116,744,554 - 116,745,631	RGD	NCBI36
Celera	7	111,765,499 - 111,766,575	RGD
HuRef	7	111,322,939 - 111,324,016	UniSTS
CRA_TCAGchr7v2	7	116,352,755 - 116,353,831	UniSTS

stSG598577

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,958,378 - 116,959,633	UniSTS	GRCh37
Build 36	7	116,745,614 - 116,746,869	RGD	NCBI36
Celera	7	111,766,558 - 111,767,813	RGD
HuRef	7	111,323,999 - 111,325,254	UniSTS
CRA_TCAGchr7v2	7	116,353,814 - 116,355,069	UniSTS

stSG598578

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,959,615 - 116,960,872	UniSTS	GRCh37
Build 36	7	116,746,851 - 116,748,108	RGD	NCBI36
Celera	7	111,767,795 - 111,769,052	RGD
HuRef	7	111,325,236 - 111,326,493	UniSTS
CRA_TCAGchr7v2	7	116,355,051 - 116,356,308	UniSTS

stSG598579

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,960,860 - 116,962,171	UniSTS	GRCh37
Build 36	7	116,748,096 - 116,749,407	RGD	NCBI36
Celera	7	111,769,040 - 111,770,351	RGD
HuRef	7	111,326,481 - 111,327,792	UniSTS
CRA_TCAGchr7v2	7	116,356,296 - 116,357,607	UniSTS

stSG598580

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,962,158 - 116,963,438	UniSTS	GRCh37
Build 36	7	116,749,394 - 116,750,674	RGD	NCBI36
Celera	7	111,770,338 - 111,771,620	RGD
HuRef	7	111,327,779 - 111,329,061	UniSTS
CRA_TCAGchr7v2	7	116,357,594 - 116,358,876	UniSTS

stSG598581

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,963,419 - 116,964,715	UniSTS	GRCh37
Build 36	7	116,750,655 - 116,751,951	RGD	NCBI36
Celera	7	111,771,601 - 111,772,897	RGD
HuRef	7	111,329,042 - 111,330,338	UniSTS
CRA_TCAGchr7v2	7	116,358,857 - 116,360,153	UniSTS

STS-X07876

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	116,917,505 - 116,917,648	UniSTS	GRCh37
Build 36	7	116,704,741 - 116,704,884	RGD	NCBI36
Celera	7	111,725,683 - 111,725,826	RGD
Cytogenetic Map	7	q31.2	UniSTS
HuRef	7	111,283,306 - 111,283,449	UniSTS
CRA_TCAGchr7v2	7	116,312,941 - 116,313,084	UniSTS
GeneMap99-GB4 RH Map	7	547.69	UniSTS
NCBI RH Map	7	1114.5	UniSTS

D7S23

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	7	q31.2	UniSTS

D7S23

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	7	q31.2	UniSTS

D7S23

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	7	q31.2	UniSTS

D7S23

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	7	q31.2	UniSTS

D7S23

Human Assembly	Chr	Position (strand)	Source	JBrowse
Cytogenetic Map	7	q31.2	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

High

Medium

173

537

Low

765

650

488

174

495

155

1955

569

1209

112

897

372

784

935

Below cutoff

1294

1743

1026

362

650

231

1661

1171

2252

188

257

494

133

363

1378

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_003391	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_024047	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC002465	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC006326	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK056742	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC029854	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC078170	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BT019608	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH236947	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471070	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CQ970106	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	GQ900909	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HF583716	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X07876	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000265441 ⟹ ENSP00000265441

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	117,275,451 - 117,323,058 (-)	Ensembl

RefSeq Acc Id:

ENST00000449446 ⟹ ENSP00000389643

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	117,277,531 - 117,323,114 (-)	Ensembl

RefSeq Acc Id:

ENST00000461427

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	117,320,469 - 117,323,152 (-)	Ensembl

RefSeq Acc Id:

ENST00000491214 ⟹ ENSP00000419466

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	117,297,726 - 117,323,041 (-)	Ensembl

RefSeq Acc Id:

ENST00000647844 ⟹ ENSP00000497695

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	117,275,451 - 117,323,099 (-)	Ensembl

RefSeq Acc Id:

NM_003391 ⟹ NP_003382

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	117,275,451 - 117,323,058 (-)	NCBI
GRCh37	7	116,916,685 - 116,963,343 (-)	ENTREZGENE
Build 36	7	116,704,518 - 116,750,579 (-)	NCBI Archive
HuRef	7	111,282,485 - 111,328,966 (-)	ENTREZGENE
CHM1_1	7	116,850,055 - 116,896,705 (-)	NCBI
T2T-CHM13v2.0	7	118,590,786 - 118,638,396 (-)	NCBI
CRA_TCAGchr7v2	7	116,312,120 - 116,358,781 (-)	ENTREZGENE

Sequence:

show sequence

GCTTCTGCTCTGGGCACGCATGGCGCCCGCACACGGAGTCTGACCTGATGCAGACGCAAGGGGG
TTAATATGAACGCCCCTCTCGGTGGAATCTGGCTCTGGCTCCCTCTGCTCTTGACCTGGCTCAC
CCCCGAGGTCAACTCTTCATGGTGGTACATGAGAGCTACAGGTGGCTCCTCCAGGGTGATGTGC
GATAATGTGCCAGGCCTGGTGAGCAGCCAGCGGCAGCTGTGTCACCGACATCCAGATGTGATGC
GTGCCATTAGCCAGGGCGTGGCCGAGTGGACAGCAGAATGCCAGCACCAGTTCCGCCAGCACCG
CTGGAATTGCAACACCCTGGACAGGGATCACAGCCTTTTTGGCAGGGTCCTACTCCGAAGTAGT
CGGGAATCTGCCTTTGTTTATGCCATCTCCTCAGCTGGAGTTGTATTTGCCATCACCAGGGCCT
GTAGCCAAGGAGAAGTAAAATCCTGTTCCTGTGATCCAAAGAAGATGGGAAGCGCCAAGGACAG
CAAAGGCATTTTTGATTGGGGTGGCTGCAGTGATAACATTGACTATGGGATCAAATTTGCCCGC
GCATTTGTGGATGCAAAGGAAAGGAAAGGAAAGGATGCCAGAGCCCTGATGAATCTTCACAACA
ACAGAGCTGGCAGGAAGGCTGTAAAGCGGTTCTTGAAACAAGAGTGCAAGTGCCACGGGGTGAG
CGGCTCATGTACTCTCAGGACATGCTGGCTGGCCATGGCCGACTTCAGGAAAACGGGCGATTAT
CTCTGGAGGAAGTACAATGGGGCCATCCAGGTGGTCATGAACCAGGATGGCACAGGTTTCACTG
TGGCTAACGAGAGGTTTAAGAAGCCAACGAAAAATGACCTCGTGTATTTTGAGAATTCTCCAGA
CTACTGTATCAGGGACCGAGAGGCAGGCTCCCTGGGTACAGCAGGCCGTGTGTGCAACCTGACT
TCCCGGGGCATGGACAGCTGTGAAGTCATGTGCTGTGGGAGAGGCTACGACACCTCCCATGTCA
CCCGGATGACCAAGTGTGGGTGTAAGTTCCACTGGTGCTGCGCCGTGCGCTGTCAGGACTGCCT
GGAAGCTCTGGATGTGCACACATGCAAGGCCCCCAAGAACGCTGACTGGACAACCGCTACATGA
CCCCAGCAGGCGTCACCATCCACCTTCCCTTCTACAAGGACTCCATTGGATCTGCAAGAACACT
GGACCTTTGGGTTCTTTCTGGGGGGATATTTCCTAAGGCATGTGGCCTTTATCTCAACGGAAGC
CCCCTCTTCCTCCCTGGGGGCCCCAGGATGGGGGGGCCACACGCTGCACCTAAAGCCTACCCTA
TTCTATCCATCTCCTGGTGTTCTGCAGTCATCTCCCCTCCTGGCGAGTTCTCTTTGGAAATAGC
ATGACAGGCTGTTCAGCCGGGAGGGTGGTGGGCCCAGACCACTGTCTCCACCCACCTTGACGTT
TCTTCTTTCTAGAGCAGTTGGCCAAGCAGAAAAAAAAGTGTCTCAAAGGAGCTTTCTCAATGTC
TTCCCACAAATGGTCCCAATTAAGAAATTCCATACTTCTCTCAGATGGGAACAGTAAAGAAAGC
AGAATCAACTGCCCCTGACTTAACTTTAACTTTTGAAAAGACCAAGACTTTTGTCTGATCAAGT
GGTTTTACAGCTACCACCCTTAGGGGTAATTGGTAATTACCTGGAGAAGAATGGCTTTCAATAC
CCTTTTAAGTTTAAAATGTGTATTTTTCAAGGCATTTATTGCCATATTAAAATCTGATGTAACA
AGGTGGGGACGTGTGTCCTTTGGTACTATGGTGTGTTGTATCTTTGTAAGAGCAAAAGCCTCAG
AAAGGGATTGCTTTGCATTACTGTCCCCTTGATATAAAAAATCTTTAGGGAATGAGAGTTCCTT
CTCACTTAGAATCCGAAGGGAATTAAAAAGAAGATGAATGGTCTGGCAATATTCTGTAACTATT
GGGTGAATATGGTGGAAAATAATTTAGTGGATGGAATATCAGAAGTATATCTGTACAGATCAAG
AAAAAAAGGGAGAATAAAATTCCTATCTCATATTATGCATGTGACCCATGGAATCTCATAACTG
AAAGACTTGAAGGATGAAAATTTTGGGGATACAAGATTGGTGAACTAAAATGCTGACAGAGAGG
TTTCCAGAGCTAACTCGTGCCTGGGGCGGCCTTACAATAAGCAGATGCCTGAAAGAAGTCGGCC
ACGTCCGCCGTCTGCTAATGCCCATCACCCTTCAAGCCCAGTTTAAAGACCTGTCATATTTAAT
TGTATTTATTTGATGCTTACAAGATGATGTGATACTGTAGCCTAAAGCAAATGACACATAGCAT
TGCTTATAAAGTTGGTAACCCTGCTATATTATATTGCAAACAAATCGTAACTTGGAGACTATGT
TTAAGGGACTCAACTGTAATTATGGGAGCATCAGTATGCAAATAGTGGTTGGCTTCTGCCATCA
GCCAAAAGATGACATTCAGGGAAAATGGAGAGGCTGCCTGCACCGTTTTTTTATGTTAAATGAA
AGAAAGGTGAAATAGCTACTTCTCGTCTTCTTGAAAAATTTGGTTCTTATTCTGTATATGACTT
CCTTACAGTGCTACATTAACAGGATATTTCATTACATGCATCTGGTATCAAATTATTGGTTCTT
CCTCATTCTTTAATACCATACAGTAAGGTCATTTAGACTGAGACTCGTACAAAACAACCTACTG
GAGTACTTTGCCATAGTTAACATTTGCCTCCAGCCCTCTTAAAAATGTCAGAATTCATCCCCTT
TCCCTCATTCCCAAATTGTTGTCTAACTTTTCCAAAGTGACTCTTTCCTCCTTTTATTCTATGG
ATTCGGATGGTGGGAACAGTGGAATGACAGTAGCTGCTCTGAGCTTGGTGTGAAGAAGGCCAGG
CACATGGGCAGCTGCTCAGTCTTCAGTTACCCTGAAGGTTGGTGTGAATTCCTTCATGAGAGTG
CGAAGGCACTTTCATGGGGGTCCCACAGCCATCAGCCCTTCCTCCTGCTGGATGAACTGTGAAA
TCATCAATCCAGGCTGTGTTTCAAATTGGAAAGGATCTTAGGAGACATCTCAGCTTCCTTTAGT
TTGGGGAAATTGAGACCAAGAGAGGCGAAGGGATTGGTGCACATATCAGGCATTGCCCAATGCT
CCATCACAAATAGGACCACACTCTTGAGTGTTTGAGATAGTGTAGGACTTTATCCATTAAATGA
AACTAGCTTCTCCCAGAATTAACTCAGTGGATTTTAAATAATTTTAGCTTCCAATGGTGTGTTT
GCTACTTTTTTTATGCCTGGTATGTTTAGATCTGACATTCTTTTTATGCTGAGATATATCCCTC
CTGGTAAGTAGCAAGGGGACAAGGATATCCACGTAGGAACCTACATAAATTGTCCTAATCCATA
AGGGAGATTATGGCAACCATCGCAAGTGGCAGTGGGTCCTGCCACTGAGGTGGGAAAAATAAGA
GAATGAAATATTGCTATCGGCTTTTACTTCTGAAAGAGGAAATGTCTATTGTTCGGGAAAAAAA
TTACACAACAAATGAAGGTAATTTTAAACTCCTTTGCCTTAGAGCTTGGTAGAGGATCAGTATT
CCAGGAACCTGAAATACACTGAAACTCTCAATTATCTGAGGCTTTTAAGGGGAATATATGGCAC
AAATTAGCCAAAACAAAATAATTGGGAAATCCCCTTATAAATTCCCTCTTTATTAAAATCTTAC
TATAAATTGAAGTTTTCTAGGTCCAAGATAATGTCCATTAATTTTCTACAATATCTGAAAAAGT
TTCCACAATAGGACAT

hide sequence

RefSeq Acc Id:

NR_024047

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	117,275,451 - 117,323,058 (-)	NCBI
GRCh37	7	116,916,685 - 116,963,343 (-)	NCBI
HuRef	7	111,282,485 - 111,328,966 (-)	ENTREZGENE
CHM1_1	7	116,850,055 - 116,896,705 (-)	NCBI
T2T-CHM13v2.0	7	118,590,786 - 118,638,396 (-)	NCBI
CRA_TCAGchr7v2	7	116,312,120 - 116,358,781 (-)	ENTREZGENE

Sequence:

show sequence

GCTTCTGCTCTGGGCACGCATGGCGCCCGCACACGGAGTCTGACCTGATGCAGACGCAAGGGGG
TTAATATGAACGCCCCTCTCGGTGGAATCTGGCTCTGGCTCCCTCTGCTCTTGACCTGGCTCAC
CCCCGAGGTCAACTCTTCATGGTGGTACATGAGAGCTACAGGTGGCTCCTCCAGGGTGATGTGC
GATAATGTGCCAGGCCTGGTGAGCAGCCAGCGGCAGCTGTGTCACCGACATCCAGATGTGATGC
GTGCCATTAGCCAGGGCGTGGCCGAGTGGACAGCAGAATGCCAGCACCAGTTCCGCCAGCACCG
CTGGAATTGCAACACCCTGGACAGGGATCACAGCCTTTTTGGCAGGGTCCTACTCCGAAGGCCT
GTAGCCAAGGAGAAGTAAAATCCTGTTCCTGTGATCCAAAGAAGATGGGAAGCGCCAAGGACAG
CAAAGGCATTTTTGATTGGGGTGGCTGCAGTGATAACATTGACTATGGGATCAAATTTGCCCGC
GCATTTGTGGATGCAAAGGAAAGGAAAGGAAAGGATGCCAGAGCCCTGATGAATCTTCACAACA
ACAGAGCTGGCAGGAAGGCTGTAAAGCGGTTCTTGAAACAAGAGTGCAAGTGCCACGGGGTGAG
CGGCTCATGTACTCTCAGGACATGCTGGCTGGCCATGGCCGACTTCAGGAAAACGGGCGATTAT
CTCTGGAGGAAGTACAATGGGGCCATCCAGGTGGTCATGAACCAGGATGGCACAGGTTTCACTG
TGGCTAACGAGAGGTTTAAGAAGCCAACGAAAAATGACCTCGTGTATTTTGAGAATTCTCCAGA
CTACTGTATCAGGGACCGAGAGGCAGGCTCCCTGGGTACAGCAGGCCGTGTGTGCAACCTGACT
TCCCGGGGCATGGACAGCTGTGAAGTCATGTGCTGTGGGAGAGGCTACGACACCTCCCATGTCA
CCCGGATGACCAAGTGTGGGTGTAAGTTCCACTGGTGCTGCGCCGTGCGCTGTCAGGACTGCCT
GGAAGCTCTGGATGTGCACACATGCAAGGCCCCCAAGAACGCTGACTGGACAACCGCTACATGA
CCCCAGCAGGCGTCACCATCCACCTTCCCTTCTACAAGGACTCCATTGGATCTGCAAGAACACT
GGACCTTTGGGTTCTTTCTGGGGGGATATTTCCTAAGGCATGTGGCCTTTATCTCAACGGAAGC
CCCCTCTTCCTCCCTGGGGGCCCCAGGATGGGGGGGCCACACGCTGCACCTAAAGCCTACCCTA
TTCTATCCATCTCCTGGTGTTCTGCAGTCATCTCCCCTCCTGGCGAGTTCTCTTTGGAAATAGC
ATGACAGGCTGTTCAGCCGGGAGGGTGGTGGGCCCAGACCACTGTCTCCACCCACCTTGACGTT
TCTTCTTTCTAGAGCAGTTGGCCAAGCAGAAAAAAAAGTGTCTCAAAGGAGCTTTCTCAATGTC
TTCCCACAAATGGTCCCAATTAAGAAATTCCATACTTCTCTCAGATGGGAACAGTAAAGAAAGC
AGAATCAACTGCCCCTGACTTAACTTTAACTTTTGAAAAGACCAAGACTTTTGTCTGATCAAGT
GGTTTTACAGCTACCACCCTTAGGGGTAATTGGTAATTACCTGGAGAAGAATGGCTTTCAATAC
CCTTTTAAGTTTAAAATGTGTATTTTTCAAGGCATTTATTGCCATATTAAAATCTGATGTAACA
AGGTGGGGACGTGTGTCCTTTGGTACTATGGTGTGTTGTATCTTTGTAAGAGCAAAAGCCTCAG
AAAGGGATTGCTTTGCATTACTGTCCCCTTGATATAAAAAATCTTTAGGGAATGAGAGTTCCTT
CTCACTTAGAATCCGAAGGGAATTAAAAAGAAGATGAATGGTCTGGCAATATTCTGTAACTATT
GGGTGAATATGGTGGAAAATAATTTAGTGGATGGAATATCAGAAGTATATCTGTACAGATCAAG
AAAAAAAGGGAGAATAAAATTCCTATCTCATATTATGCATGTGACCCATGGAATCTCATAACTG
AAAGACTTGAAGGATGAAAATTTTGGGGATACAAGATTGGTGAACTAAAATGCTGACAGAGAGG
TTTCCAGAGCTAACTCGTGCCTGGGGCGGCCTTACAATAAGCAGATGCCTGAAAGAAGTCGGCC
ACGTCCGCCGTCTGCTAATGCCCATCACCCTTCAAGCCCAGTTTAAAGACCTGTCATATTTAAT
TGTATTTATTTGATGCTTACAAGATGATGTGATACTGTAGCCTAAAGCAAATGACACATAGCAT
TGCTTATAAAGTTGGTAACCCTGCTATATTATATTGCAAACAAATCGTAACTTGGAGACTATGT
TTAAGGGACTCAACTGTAATTATGGGAGCATCAGTATGCAAATAGTGGTTGGCTTCTGCCATCA
GCCAAAAGATGACATTCAGGGAAAATGGAGAGGCTGCCTGCACCGTTTTTTTATGTTAAATGAA
AGAAAGGTGAAATAGCTACTTCTCGTCTTCTTGAAAAATTTGGTTCTTATTCTGTATATGACTT
CCTTACAGTGCTACATTAACAGGATATTTCATTACATGCATCTGGTATCAAATTATTGGTTCTT
CCTCATTCTTTAATACCATACAGTAAGGTCATTTAGACTGAGACTCGTACAAAACAACCTACTG
GAGTACTTTGCCATAGTTAACATTTGCCTCCAGCCCTCTTAAAAATGTCAGAATTCATCCCCTT
TCCCTCATTCCCAAATTGTTGTCTAACTTTTCCAAAGTGACTCTTTCCTCCTTTTATTCTATGG
ATTCGGATGGTGGGAACAGTGGAATGACAGTAGCTGCTCTGAGCTTGGTGTGAAGAAGGCCAGG
CACATGGGCAGCTGCTCAGTCTTCAGTTACCCTGAAGGTTGGTGTGAATTCCTTCATGAGAGTG
CGAAGGCACTTTCATGGGGGTCCCACAGCCATCAGCCCTTCCTCCTGCTGGATGAACTGTGAAA
TCATCAATCCAGGCTGTGTTTCAAATTGGAAAGGATCTTAGGAGACATCTCAGCTTCCTTTAGT
TTGGGGAAATTGAGACCAAGAGAGGCGAAGGGATTGGTGCACATATCAGGCATTGCCCAATGCT
CCATCACAAATAGGACCACACTCTTGAGTGTTTGAGATAGTGTAGGACTTTATCCATTAAATGA
AACTAGCTTCTCCCAGAATTAACTCAGTGGATTTTAAATAATTTTAGCTTCCAATGGTGTGTTT
GCTACTTTTTTTATGCCTGGTATGTTTAGATCTGACATTCTTTTTATGCTGAGATATATCCCTC
CTGGTAAGTAGCAAGGGGACAAGGATATCCACGTAGGAACCTACATAAATTGTCCTAATCCATA
AGGGAGATTATGGCAACCATCGCAAGTGGCAGTGGGTCCTGCCACTGAGGTGGGAAAAATAAGA
GAATGAAATATTGCTATCGGCTTTTACTTCTGAAAGAGGAAATGTCTATTGTTCGGGAAAAAAA
TTACACAACAAATGAAGGTAATTTTAAACTCCTTTGCCTTAGAGCTTGGTAGAGGATCAGTATT
CCAGGAACCTGAAATACACTGAAACTCTCAATTATCTGAGGCTTTTAAGGGGAATATATGGCAC
AAATTAGCCAAAACAAAATAATTGGGAAATCCCCTTATAAATTCCCTCTTTATTAAAATCTTAC
TATAAATTGAAGTTTTCTAGGTCCAAGATAATGTCCATTAATTTTCTACAATATCTGAAAAAGT
TTCCACAATAGGACAT

hide sequence

Protein Sequences


Protein RefSeqs	NP_003382	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAB67043	(Get FASTA)	NCBI Sequence Viewer
	AAD28351	(Get FASTA)	NCBI Sequence Viewer
	AAH29854	(Get FASTA)	NCBI Sequence Viewer
	AAH78170	(Get FASTA)	NCBI Sequence Viewer
	AAV38415	(Get FASTA)	NCBI Sequence Viewer
	ADO22426	(Get FASTA)	NCBI Sequence Viewer
	BAG51800	(Get FASTA)	NCBI Sequence Viewer
	CAA30725	(Get FASTA)	NCBI Sequence Viewer
	CAI38640	(Get FASTA)	NCBI Sequence Viewer
	CCQ43213	(Get FASTA)	NCBI Sequence Viewer
	EAL24355	(Get FASTA)	NCBI Sequence Viewer
	EAW83525	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000265441
	ENSP00000265441.3
	ENSP00000389643.1
	ENSP00000419466.1
	ENSP00000497695.1
GenBank Protein	P09544	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_003382 ⟸ NM_003391
- Peptide Label:	precursor
- UniProtKB:	Q75N05 (UniProtKB/Swiss-Prot), A4D0V1 (UniProtKB/Swiss-Prot), Q9UDP9 (UniProtKB/Swiss-Prot), P09544 (UniProtKB/Swiss-Prot), A0A384MDX3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MNAPLGGIWLWLPLLLTWLTPEVNSSWWYMRATGGSSRVMCDNVPGLVSSQRQLCHRHPDVMRA ISQGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAISSAGVVFAITRACS QGEVKSCSCDPKKMGSAKDSKGIFDWGGCSDNIDYGIKFARAFVDAKERKGKDARALMNLHNNR AGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNGAIQVVMNQDGTGFTVA NERFKKPTKNDLVYFENSPDYCIRDREAGSLGTAGRVCNLTSRGMDSCEVMCCGRGYDTSHVTR MTKCGCKFHWCCAVRCQDCLEALDVHTCKAPKNADWTTAT hide sequence

RefSeq Acc Id:

ENSP00000419466 ⟸ ENST00000491214

RefSeq Acc Id:

ENSP00000389643 ⟸ ENST00000449446

RefSeq Acc Id:

ENSP00000265441 ⟸ ENST00000265441

RefSeq Acc Id:

ENSP00000497695 ⟸ ENST00000647844

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P09544-F1-model_v2	AlphaFold	P09544	1-360	view protein structure

Promoters

RGD ID:

7211759

Promoter ID:

EPDNEW_H11626

Type:

initiation region

Name:

WNT2_2

Description:

Wnt family member 2

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H11627

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	117,323,058 - 117,323,118	EPDNEW

RGD ID:

7211763

Promoter ID:

EPDNEW_H11627

Type:

initiation region

Name:

WNT2_1

Description:

Wnt family member 2

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H11626

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	117,323,286 - 117,323,346	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:12780	AgrOrtholog
COSMIC	WNT2	COSMIC
Ensembl Genes	ENSG00000105989	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000265441	ENTREZGENE
	ENST00000265441.8	UniProtKB/Swiss-Prot
	ENST00000449446.5	UniProtKB/TrEMBL
	ENST00000491214.1	UniProtKB/TrEMBL
	ENST00000647844	ENTREZGENE
	ENST00000647844.1	UniProtKB/TrEMBL
Gene3D-CATH	3.30.2460.20	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000105989	GTEx
HGNC ID	HGNC:12780	ENTREZGENE
Human Proteome Map	WNT2	Human Proteome Map
InterPro	Wnt	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Wnt2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Wnt_C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Wnt_CS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:7472	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	7472	ENTREZGENE
OMIM	147870	OMIM
PANTHER	PROTEIN WNT-2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR12027	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	wnt	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA37381	PharmGKB
PRINTS	WNT2PROTEIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	WNTPROTEIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE	WNT1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	WNT1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A384MDX3	ENTREZGENE, UniProtKB/TrEMBL
	A0A3B3ITC9_HUMAN	UniProtKB/TrEMBL
	A4D0V1	ENTREZGENE
	C9JUI2_HUMAN	UniProtKB/TrEMBL
	F8WDR1_HUMAN	UniProtKB/TrEMBL
	L8EA39_HUMAN	UniProtKB/TrEMBL
	P09544	ENTREZGENE
	Q75N05	ENTREZGENE
	Q9UDP9	ENTREZGENE
	WNT2_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	A4D0V1	UniProtKB/Swiss-Prot
	Q75N05	UniProtKB/Swiss-Prot
	Q9UDP9	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-03-28	WNT2	Wnt family member 2	WNT2	wingless-type MMTV integration site family member 2	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

RGD Manual Annotations

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

RGD Manual Annotations

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - ClinVar