ASZ1 (ankyrin repeat, SAM and basic leucine zipper domain containing 1) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: ASZ1 (ankyrin repeat, SAM and basic leucine zipper domain containing 1) Homo sapiens
Analyze
Symbol: ASZ1
Name: ankyrin repeat, SAM and basic leucine zipper domain containing 1
RGD ID: 1348719
HGNC Page HGNC:1350
Description: Predicted to be involved in male meiotic nuclear division; retrotransposon silencing; and spermatogenesis. Predicted to be located in cytoplasm. Predicted to be active in pi-body.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: 4933400N19Rik; ALP1; ANKL1; ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1; ankyrin-like 1; ankyrin-like protein 1; C7orf7; CT1.19; GASZ; germ cell-specific ankyrin, SAM and basic leucine zipper domain-containing protein; MGC26634; Orf3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387117,363,222 - 117,427,493 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7117,363,222 - 117,428,123 (-)EnsemblGRCh38hg38GRCh38
GRCh377117,003,276 - 117,067,547 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367116,790,512 - 116,854,779 (-)NCBINCBI36Build 36hg18NCBI36
Build 347116,597,226 - 116,661,494NCBI
Celera7111,811,458 - 111,875,763 (-)NCBICelera
Cytogenetic Map7q31.2NCBI
HuRef7111,368,899 - 111,433,205 (-)NCBIHuRef
CHM1_17116,936,638 - 117,000,932 (-)NCBICHM1_1
T2T-CHM13v2.07118,678,562 - 118,742,828 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27116,398,714 - 116,463,018 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IEA,ISS)
pi-body  (IBA,IEA,ISS)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Identification of Gasz, an evolutionarily conserved gene expressed exclusively in germ cells and encoding a protein with four ankyrin repeats, a sterile-alpha motif, and a basic leucine zipper. Yan W, etal., Mol Endocrinol 2002 Jun;16(6):1168-84.
Additional References at PubMed
PMID:11279520   PMID:12477932   PMID:12690205   PMID:14702039   PMID:15364959   PMID:15489334   PMID:21378990   PMID:21873635   PMID:21880841   PMID:23816659   PMID:23966867   PMID:32296183  
PMID:36217029  


Genomics

Comparative Map Data
ASZ1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387117,363,222 - 117,427,493 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7117,363,222 - 117,428,123 (-)EnsemblGRCh38hg38GRCh38
GRCh377117,003,276 - 117,067,547 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367116,790,512 - 116,854,779 (-)NCBINCBI36Build 36hg18NCBI36
Build 347116,597,226 - 116,661,494NCBI
Celera7111,811,458 - 111,875,763 (-)NCBICelera
Cytogenetic Map7q31.2NCBI
HuRef7111,368,899 - 111,433,205 (-)NCBIHuRef
CHM1_17116,936,638 - 117,000,932 (-)NCBICHM1_1
T2T-CHM13v2.07118,678,562 - 118,742,828 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27116,398,714 - 116,463,018 (-)NCBI
Asz1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39618,050,963 - 18,109,060 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl618,050,963 - 18,109,060 (-)EnsemblGRCm39 Ensembl
GRCm38618,050,964 - 18,109,061 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl618,050,964 - 18,109,061 (-)EnsemblGRCm38mm10GRCm38
MGSCv37618,000,964 - 18,059,061 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36618,000,972 - 18,059,055 (-)NCBIMGSCv36mm8
Celera618,131,967 - 18,189,690 (-)NCBICelera
Cytogenetic Map6A2NCBI
cM Map68.09NCBI
Asz1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8447,366,373 - 47,421,976 (-)NCBIGRCr8
mRatBN7.2446,400,485 - 46,456,085 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl446,400,485 - 46,456,085 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx451,387,964 - 51,450,415 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0447,309,065 - 47,371,511 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0445,724,300 - 45,786,771 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0445,358,574 - 45,414,177 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl445,358,574 - 45,414,177 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0445,962,482 - 46,018,085 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4443,715,678 - 43,771,281 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1443,885,569 - 43,941,174 (-)NCBI
Celera441,667,469 - 41,722,729 (-)NCBICelera
Cytogenetic Map4q22NCBI
Asz1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543223,060,657 - 23,119,427 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495543223,059,462 - 23,119,421 (-)NCBIChiLan1.0ChiLan1.0
ASZ1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26154,190,912 - 154,262,880 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan176,201,171 - 6,267,635 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v07109,330,983 - 109,397,864 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.17122,025,741 - 122,091,923 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7122,025,611 - 122,091,923 (-)Ensemblpanpan1.1panPan2
ASZ1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11456,197,784 - 56,250,067 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1456,197,875 - 56,250,073 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1455,593,174 - 55,645,421 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01456,237,329 - 56,289,866 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1456,237,416 - 56,289,872 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11456,269,361 - 56,321,897 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01455,956,693 - 56,008,911 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01456,328,130 - 56,380,667 (-)NCBIUU_Cfam_GSD_1.0
Asz1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511844,890,143 - 44,933,250 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365891,756,616 - 1,799,580 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365891,756,616 - 1,799,810 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ASZ1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1828,859,112 - 28,910,934 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11828,859,140 - 28,910,927 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21830,593,587 - 30,641,161 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ASZ1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12186,042,400 - 86,108,247 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2186,042,691 - 86,107,099 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604217,624,753 - 17,689,593 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Asz1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248271,944,534 - 1,998,281 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ASZ1
28 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_130768.2(ASZ1):c.440+5186A>G single nucleotide variant Lung cancer [RCV000105444] Chr7:117414977 [GRCh38]
Chr7:117055031 [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 7q31.2-33(chr7:117326805-134790689)x1 copy number loss See cases [RCV000138226] Chr7:117326805..134790689 [GRCh38]
Chr7:116966859..134475440 [GRCh37]
Chr7:116754095..134125980 [NCBI36]
Chr7:7q31.2-33		 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
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34		 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
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
NM_130768.3(ASZ1):c.16C>G (p.Leu6Val) single nucleotide variant Inborn genetic diseases [RCV003296166] Chr7:117427445 [GRCh38]
Chr7:117067499 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.410C>T (p.Ser137Leu) single nucleotide variant Inborn genetic diseases [RCV003261104] Chr7:117420193 [GRCh38]
Chr7:117060247 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.457A>G (p.Ile153Val) single nucleotide variant Inborn genetic diseases [RCV003252063] Chr7:117385793 [GRCh38]
Chr7:117025847 [GRCh37]
Chr7:7q31.2		 uncertain significance
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
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
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(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_130768.3(ASZ1):c.117G>A (p.Arg39=) single nucleotide variant not provided [RCV000969952] Chr7:117426924 [GRCh38]
Chr7:117066978 [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
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
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
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NC_000007.13:g.(?_116339139)_(117307162_?)del deletion Renal cell carcinoma [RCV001343585] Chr7:116339139..117307162 [GRCh37]
Chr7:7q31.2		 uncertain significance
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
Single allele deletion Delayed speech and language development [RCV002251690] Chr7:114888786..124720929 [GRCh37]
Chr7:7q31.2-31.33		 likely 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
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 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_130768.3(ASZ1):c.922A>G (p.Met308Val) single nucleotide variant Inborn genetic diseases [RCV002836646] Chr7:117381034 [GRCh38]
Chr7:117021088 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.1288C>T (p.Arg430Trp) single nucleotide variant Inborn genetic diseases [RCV002779757] Chr7:117363736 [GRCh38]
Chr7:117003790 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.1148T>G (p.Val383Gly) single nucleotide variant Inborn genetic diseases [RCV002785070] Chr7:117368625 [GRCh38]
Chr7:117008679 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.64G>T (p.Asp22Tyr) single nucleotide variant Inborn genetic diseases [RCV002660690] Chr7:117427397 [GRCh38]
Chr7:117067451 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.727G>C (p.Gly243Arg) single nucleotide variant Inborn genetic diseases [RCV002798987] Chr7:117383071 [GRCh38]
Chr7:117023125 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.460A>G (p.Met154Val) single nucleotide variant Inborn genetic diseases [RCV002704644] Chr7:117385790 [GRCh38]
Chr7:117025844 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.301A>G (p.Arg101Gly) single nucleotide variant Inborn genetic diseases [RCV002803119] Chr7:117422264 [GRCh38]
Chr7:117062318 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.662T>C (p.Ile221Thr) single nucleotide variant Inborn genetic diseases [RCV002987288] Chr7:117384751 [GRCh38]
Chr7:117024805 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.189G>C (p.Gln63His) single nucleotide variant Inborn genetic diseases [RCV002873951] Chr7:117426852 [GRCh38]
Chr7:117066906 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.8C>G (p.Ala3Gly) single nucleotide variant Inborn genetic diseases [RCV002744380] Chr7:117427453 [GRCh38]
Chr7:117067507 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.1091A>G (p.Asn364Ser) single nucleotide variant Inborn genetic diseases [RCV002669004] Chr7:117368682 [GRCh38]
Chr7:117008736 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.1048G>A (p.Glu350Lys) single nucleotide variant Inborn genetic diseases [RCV002959967] Chr7:117379945 [GRCh38]
Chr7:117019999 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.64G>C (p.Asp22His) single nucleotide variant Inborn genetic diseases [RCV002941368] Chr7:117427397 [GRCh38]
Chr7:117067451 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.272A>G (p.Asn91Ser) single nucleotide variant Inborn genetic diseases [RCV002657478] Chr7:117422293 [GRCh38]
Chr7:117062347 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.14C>G (p.Ala5Gly) single nucleotide variant Inborn genetic diseases [RCV002724459] Chr7:117427447 [GRCh38]
Chr7:117067501 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.266T>C (p.Val89Ala) single nucleotide variant Inborn genetic diseases [RCV003204066] Chr7:117422299 [GRCh38]
Chr7:117062353 [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
NM_130768.3(ASZ1):c.754G>A (p.Asp252Asn) single nucleotide variant Inborn genetic diseases [RCV003309383] Chr7:117383044 [GRCh38]
Chr7:117023098 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.55G>C (p.Glu19Gln) single nucleotide variant Inborn genetic diseases [RCV003374555] Chr7:117427406 [GRCh38]
Chr7:117067460 [GRCh37]
Chr7:7q31.2		 uncertain significance
NM_130768.3(ASZ1):c.1056T>C (p.Ser352=) single nucleotide variant Inborn genetic diseases [RCV003367164] Chr7:117368717 [GRCh38]
Chr7:117008771 [GRCh37]
Chr7:7q31.2		 likely benign
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:750
Count of miRNA genes:424
Interacting mature miRNAs:466
Transcripts:ENST00000284629, ENST00000428663, ENST00000450714, ENST00000463182, ENST00000465832, ENST00000479454
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
D6S409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,010,785 - 117,010,954UniSTSGRCh37
GRCh376143,517,394 - 143,517,565UniSTSGRCh37
Build 366143,559,087 - 143,559,258RGDNCBI36
Celera6144,257,801 - 144,257,972RGD
Celera7111,818,967 - 111,819,136UniSTS
Cytogenetic Map7q31.2UniSTS
HuRef7111,376,408 - 111,376,577UniSTS
HuRef6141,081,456 - 141,081,625UniSTS
CRA_TCAGchr7v27116,406,223 - 116,406,392UniSTS
Marshfield Genetic Map6144.46RGD
Marshfield Genetic Map7124.08UniSTS
Genethon Genetic Map7125.2UniSTS
deCODE Assembly Map7123.6UniSTS
Whitehead-YAC Contig Map7 UniSTS
D7S633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,010,755 - 117,010,814UniSTSGRCh37
Celera7111,818,937 - 111,818,996UniSTS
Cytogenetic Map7q31.2UniSTS
HuRef7111,376,378 - 111,376,437UniSTS
CRA_TCAGchr7v27116,406,193 - 116,406,252UniSTS
Marshfield Genetic Map7124.08RGD
RH123968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,068,302 - 117,068,651UniSTSGRCh37
Build 367116,855,538 - 116,855,887RGDNCBI36
Celera7111,876,488 - 111,876,837RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,433,930 - 111,434,279UniSTS
CRA_TCAGchr7v27116,463,743 - 116,464,092UniSTS
TNG Radiation Hybrid Map752321.0UniSTS
ECD00547  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,049,538 - 117,050,438UniSTSGRCh37
Build 367116,836,774 - 116,837,674RGDNCBI36
Celera7111,857,724 - 111,858,624RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,415,165 - 111,416,065UniSTS
CRA_TCAGchr7v27116,444,980 - 116,445,880UniSTS
ECD03949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,019,582 - 117,020,361UniSTSGRCh37
Build 367116,806,818 - 116,807,597RGDNCBI36
Celera7111,827,764 - 111,828,543RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,385,205 - 111,385,984UniSTS
CRA_TCAGchr7v27116,415,020 - 116,415,799UniSTS
ECD04244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,006,736 - 117,007,506UniSTSGRCh37
Build 367116,793,972 - 116,794,742RGDNCBI36
Celera7111,814,918 - 111,815,688RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,372,359 - 111,373,129UniSTS
CRA_TCAGchr7v27116,402,174 - 116,402,944UniSTS
ECD04359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,050,594 - 117,051,360UniSTSGRCh37
Build 367116,837,830 - 116,838,596RGDNCBI36
Celera7111,858,780 - 111,859,546RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,416,221 - 111,416,987UniSTS
CRA_TCAGchr7v27116,446,036 - 116,446,802UniSTS
ECD04566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,056,861 - 117,057,621UniSTSGRCh37
Build 367116,844,097 - 116,844,857RGDNCBI36
Celera7111,865,047 - 111,865,807RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,422,488 - 111,423,248UniSTS
CRA_TCAGchr7v27116,452,303 - 116,453,063UniSTS
ECD04878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,023,594 - 117,024,345UniSTSGRCh37
Build 367116,810,830 - 116,811,581RGDNCBI36
Celera7111,831,776 - 111,832,527RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,389,217 - 111,389,968UniSTS
CRA_TCAGchr7v27116,419,032 - 116,419,783UniSTS
ECD05135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,003,659 - 117,004,403UniSTSGRCh37
Build 367116,790,895 - 116,791,639RGDNCBI36
Celera7111,811,841 - 111,812,585RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,369,282 - 111,370,026UniSTS
CRA_TCAGchr7v27116,399,097 - 116,399,841UniSTS
ECD05902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,024,520 - 117,025,243UniSTSGRCh37
Build 367116,811,756 - 116,812,479RGDNCBI36
Celera7111,832,702 - 111,833,425RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,390,143 - 111,390,866UniSTS
CRA_TCAGchr7v27116,419,958 - 116,420,681UniSTS
ECD06081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,011,169 - 117,011,887UniSTSGRCh37
Build 367116,798,405 - 116,799,123RGDNCBI36
Celera7111,819,351 - 111,820,069RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,376,792 - 111,377,510UniSTS
CRA_TCAGchr7v27116,406,607 - 116,407,325UniSTS
ECD06328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,057,652 - 117,058,363UniSTSGRCh37
Build 367116,844,888 - 116,845,599RGDNCBI36
Celera7111,865,838 - 111,866,549RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,423,279 - 111,423,990UniSTS
CRA_TCAGchr7v27116,453,094 - 116,453,805UniSTS
ECD07596  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,008,358 - 117,009,035UniSTSGRCh37
Build 367116,795,594 - 116,796,271RGDNCBI36
Celera7111,816,540 - 111,817,217RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,373,981 - 111,374,658UniSTS
CRA_TCAGchr7v27116,403,796 - 116,404,473UniSTS
ECD08839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,013,868 - 117,014,512UniSTSGRCh37
Build 367116,801,104 - 116,801,748RGDNCBI36
Celera7111,822,050 - 111,822,694RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,379,491 - 111,380,135UniSTS
CRA_TCAGchr7v27116,409,306 - 116,409,950UniSTS
ECD08840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,022,654 - 117,023,298UniSTSGRCh37
Build 367116,809,890 - 116,810,534RGDNCBI36
Celera7111,830,836 - 111,831,480RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,388,277 - 111,388,921UniSTS
CRA_TCAGchr7v27116,418,092 - 116,418,736UniSTS
ECD09264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,035,143 - 117,035,776UniSTSGRCh37
Build 367116,822,379 - 116,823,012RGDNCBI36
Celera7111,843,325 - 111,843,958RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,400,766 - 111,401,399UniSTS
CRA_TCAGchr7v27116,430,581 - 116,431,214UniSTS
ECD09733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,033,539 - 117,034,160UniSTSGRCh37
Build 367116,820,775 - 116,821,396RGDNCBI36
Celera7111,841,721 - 111,842,342RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,399,162 - 111,399,783UniSTS
CRA_TCAGchr7v27116,428,977 - 116,429,598UniSTS
ECD09778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,062,310 - 117,062,930UniSTSGRCh37
Build 367116,849,546 - 116,850,166RGDNCBI36
Celera7111,870,495 - 111,871,115RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,427,937 - 111,428,557UniSTS
CRA_TCAGchr7v27116,457,750 - 116,458,370UniSTS
ECD10006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,064,276 - 117,064,889UniSTSGRCh37
Build 367116,851,512 - 116,852,125RGDNCBI36
Celera7111,872,461 - 111,873,074RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,429,903 - 111,430,516UniSTS
CRA_TCAGchr7v27116,459,716 - 116,460,329UniSTS
ECD10233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,067,280 - 117,067,887UniSTSGRCh37
Build 367116,854,516 - 116,855,123RGDNCBI36
Celera7111,875,466 - 111,876,073RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,432,908 - 111,433,515UniSTS
CRA_TCAGchr7v27116,462,721 - 116,463,328UniSTS
ECD10301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,066,621 - 117,067,226UniSTSGRCh37
Build 367116,853,857 - 116,854,462RGDNCBI36
Celera7111,874,807 - 111,875,412RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,432,249 - 111,432,854UniSTS
CRA_TCAGchr7v27116,462,062 - 116,462,667UniSTS
ECD10343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,067,971 - 117,068,575UniSTSGRCh37
Build 367116,855,207 - 116,855,811RGDNCBI36
Celera7111,876,157 - 111,876,761RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,433,599 - 111,434,203UniSTS
CRA_TCAGchr7v27116,463,412 - 116,464,016UniSTS
ECD11636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,021,075 - 117,021,641UniSTSGRCh37
Build 367116,808,311 - 116,808,877RGDNCBI36
Celera7111,829,257 - 111,829,823RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,386,698 - 111,387,264UniSTS
CRA_TCAGchr7v27116,416,513 - 116,417,079UniSTS
ECD11637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,021,885 - 117,022,451UniSTSGRCh37
Build 367116,809,121 - 116,809,687RGDNCBI36
Celera7111,830,067 - 111,830,633RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,387,508 - 111,388,074UniSTS
CRA_TCAGchr7v27116,417,323 - 116,417,889UniSTS
ECD11735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,020,451 - 117,021,014UniSTSGRCh37
Build 367116,807,687 - 116,808,250RGDNCBI36
Celera7111,828,633 - 111,829,196RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,386,074 - 111,386,637UniSTS
CRA_TCAGchr7v27116,415,889 - 116,416,452UniSTS
ECD11901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,040,519 - 117,041,077UniSTSGRCh37
Build 367116,827,755 - 116,828,313RGDNCBI36
Celera7111,848,701 - 111,849,259RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,406,142 - 111,406,700UniSTS
CRA_TCAGchr7v27116,435,957 - 116,436,515UniSTS
ECD12305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,052,210 - 117,052,757UniSTSGRCh37
Build 367116,839,446 - 116,839,993RGDNCBI36
Celera7111,860,396 - 111,860,943RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,417,837 - 111,418,384UniSTS
CRA_TCAGchr7v27116,447,652 - 116,448,199UniSTS
ECD13614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,026,460 - 117,026,973UniSTSGRCh37
Build 367116,813,696 - 116,814,209RGDNCBI36
Celera7111,834,642 - 111,835,155RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,392,083 - 111,392,596UniSTS
CRA_TCAGchr7v27116,421,898 - 116,422,411UniSTS
ECD14804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,004,781 - 117,005,266UniSTSGRCh37
Build 367116,792,017 - 116,792,502RGDNCBI36
Celera7111,812,963 - 111,813,448RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,370,404 - 111,370,889UniSTS
CRA_TCAGchr7v27116,400,219 - 116,400,704UniSTS
ECD15233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,059,900 - 117,060,375UniSTSGRCh37
Build 367116,847,136 - 116,847,611RGDNCBI36
Celera7111,868,085 - 111,868,560RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,425,527 - 111,426,002UniSTS
CRA_TCAGchr7v27116,455,340 - 116,455,815UniSTS
ECD15422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,014,807 - 117,015,277UniSTSGRCh37
Build 367116,802,043 - 116,802,513RGDNCBI36
Celera7111,822,989 - 111,823,459RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,380,430 - 111,380,900UniSTS
CRA_TCAGchr7v27116,410,245 - 116,410,715UniSTS
ECD15684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,005,338 - 117,005,802UniSTSGRCh37
Build 367116,792,574 - 116,793,038RGDNCBI36
Celera7111,813,520 - 111,813,984RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,370,961 - 111,371,425UniSTS
CRA_TCAGchr7v27116,400,776 - 116,401,240UniSTS
ECD15846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,010,348 - 117,010,808UniSTSGRCh37
Build 367116,797,584 - 116,798,044RGDNCBI36
Celera7111,818,530 - 111,818,990RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,375,971 - 111,376,431UniSTS
CRA_TCAGchr7v27116,405,786 - 116,406,246UniSTS
ECD16673  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,052,873 - 117,053,303UniSTSGRCh37
Build 367116,840,109 - 116,840,539RGDNCBI36
Celera7111,861,059 - 111,861,489RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,418,500 - 111,418,930UniSTS
CRA_TCAGchr7v27116,448,315 - 116,448,745UniSTS
ECD16973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,061,837 - 117,062,254UniSTSGRCh37
Build 367116,849,073 - 116,849,490RGDNCBI36
Celera7111,870,022 - 111,870,439RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,427,464 - 111,427,881UniSTS
CRA_TCAGchr7v27116,457,277 - 116,457,694UniSTS
ECD17516  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,025,743 - 117,026,138UniSTSGRCh37
Build 367116,812,979 - 116,813,374RGDNCBI36
Celera7111,833,925 - 111,834,320RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,391,366 - 111,391,761UniSTS
CRA_TCAGchr7v27116,421,181 - 116,421,576UniSTS
ECD18274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,063,216 - 117,063,582UniSTSGRCh37
Build 367116,850,452 - 116,850,818RGDNCBI36
Celera7111,871,401 - 111,871,767RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,428,843 - 111,429,209UniSTS
CRA_TCAGchr7v27116,458,656 - 116,459,022UniSTS
ECD18342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,039,289 - 117,039,652UniSTSGRCh37
Build 367116,826,525 - 116,826,888RGDNCBI36
Celera7111,847,471 - 111,847,834RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,404,912 - 111,405,275UniSTS
CRA_TCAGchr7v27116,434,727 - 116,435,090UniSTS
ECD18451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,059,396 - 117,059,755UniSTSGRCh37
Build 367116,846,632 - 116,846,991RGDNCBI36
Celera7111,867,581 - 111,867,940RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,425,023 - 111,425,382UniSTS
CRA_TCAGchr7v27116,454,836 - 116,455,195UniSTS
ECD19324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,060,650 - 117,060,975UniSTSGRCh37
Build 367116,847,886 - 116,848,211RGDNCBI36
Celera7111,868,835 - 111,869,160RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,426,277 - 111,426,602UniSTS
CRA_TCAGchr7v27116,456,090 - 116,456,415UniSTS
ECD20801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,013,478 - 117,013,749UniSTSGRCh37
Build 367116,800,714 - 116,800,985RGDNCBI36
Celera7111,821,660 - 111,821,931RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,379,101 - 111,379,372UniSTS
CRA_TCAGchr7v27116,408,916 - 116,409,187UniSTS
ECD20802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,040,065 - 117,040,336UniSTSGRCh37
Build 367116,827,301 - 116,827,572RGDNCBI36
Celera7111,848,247 - 111,848,518RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,405,688 - 111,405,959UniSTS
CRA_TCAGchr7v27116,435,503 - 116,435,774UniSTS
ECD21577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,038,583 - 117,038,828UniSTSGRCh37
Build 367116,825,819 - 116,826,064RGDNCBI36
Celera7111,846,765 - 111,847,010RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,404,206 - 111,404,451UniSTS
CRA_TCAGchr7v27116,434,021 - 116,434,266UniSTS
ECD21761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,007,691 - 117,007,931UniSTSGRCh37
Build 367116,794,927 - 116,795,167RGDNCBI36
Celera7111,815,873 - 111,816,113RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,373,314 - 111,373,554UniSTS
CRA_TCAGchr7v27116,403,129 - 116,403,369UniSTS
ECD23316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,053,510 - 117,053,702UniSTSGRCh37
Build 367116,840,746 - 116,840,938RGDNCBI36
Celera7111,861,696 - 111,861,888RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,419,137 - 111,419,329UniSTS
CRA_TCAGchr7v27116,448,952 - 116,449,144UniSTS
ECD23430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,004,527 - 117,004,716UniSTSGRCh37
Build 367116,791,763 - 116,791,952RGDNCBI36
Celera7111,812,709 - 111,812,898RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,370,150 - 111,370,339UniSTS
CRA_TCAGchr7v27116,399,965 - 116,400,154UniSTS
ECD24331  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,049,099 - 117,049,240UniSTSGRCh37
Build 367116,836,335 - 116,836,476RGDNCBI36
Celera7111,857,285 - 111,857,426RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,414,726 - 111,414,867UniSTS
CRA_TCAGchr7v27116,444,541 - 116,444,682UniSTS
ECD24373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,053,834 - 117,053,971UniSTSGRCh37
Build 367116,841,070 - 116,841,207RGDNCBI36
Celera7111,862,020 - 111,862,157RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,419,461 - 111,419,598UniSTS
CRA_TCAGchr7v27116,449,276 - 116,449,413UniSTS
ECD24452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,066,059 - 117,066,183UniSTSGRCh37
Build 367116,853,295 - 116,853,419RGDNCBI36
Celera7111,874,245 - 111,874,369RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,431,687 - 111,431,811UniSTS
CRA_TCAGchr7v27116,461,500 - 116,461,624UniSTS
REN63571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,069,251 - 117,069,481UniSTSGRCh37
Build 367116,856,487 - 116,856,717RGDNCBI36
Celera7111,877,437 - 111,877,667RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,434,879 - 111,435,109UniSTS
CRA_TCAGchr7v27116,464,692 - 116,464,922UniSTS
REN63572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,069,033 - 117,069,264UniSTSGRCh37
Build 367116,856,269 - 116,856,500RGDNCBI36
Celera7111,877,219 - 111,877,450RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,434,661 - 111,434,892UniSTS
CRA_TCAGchr7v27116,464,474 - 116,464,705UniSTS
REN63573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,068,782 - 117,069,028UniSTSGRCh37
Build 367116,856,018 - 116,856,264RGDNCBI36
Celera7111,876,968 - 111,877,214RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,434,410 - 111,434,656UniSTS
CRA_TCAGchr7v27116,464,223 - 116,464,469UniSTS
REN63574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,068,564 - 117,068,800UniSTSGRCh37
Build 367116,855,800 - 116,856,036RGDNCBI36
Celera7111,876,750 - 111,876,986RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,434,192 - 111,434,428UniSTS
CRA_TCAGchr7v27116,464,005 - 116,464,241UniSTS
REN63575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,068,314 - 117,068,569UniSTSGRCh37
Build 367116,855,550 - 116,855,805RGDNCBI36
Celera7111,876,500 - 111,876,755RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,433,942 - 111,434,197UniSTS
CRA_TCAGchr7v27116,463,755 - 116,464,010UniSTS
REN63576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,068,088 - 117,068,332UniSTSGRCh37
Build 367116,855,324 - 116,855,568RGDNCBI36
Celera7111,876,274 - 111,876,518RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,433,716 - 111,433,960UniSTS
CRA_TCAGchr7v27116,463,529 - 116,463,773UniSTS
REN63577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,067,863 - 117,068,088UniSTSGRCh37
Build 367116,855,099 - 116,855,324RGDNCBI36
Celera7111,876,049 - 111,876,274RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,433,491 - 111,433,716UniSTS
CRA_TCAGchr7v27116,463,304 - 116,463,529UniSTS
REN63578  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,067,592 - 117,067,853UniSTSGRCh37
Build 367116,854,828 - 116,855,089RGDNCBI36
Celera7111,875,778 - 111,876,039RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,433,220 - 111,433,481UniSTS
CRA_TCAGchr7v27116,463,033 - 116,463,294UniSTS
REN63579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,067,373 - 117,067,610UniSTSGRCh37
Build 367116,854,609 - 116,854,846RGDNCBI36
Celera7111,875,559 - 111,875,796RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,433,001 - 111,433,238UniSTS
CRA_TCAGchr7v27116,462,814 - 116,463,051UniSTS
REN63580  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,067,147 - 117,067,392UniSTSGRCh37
Build 367116,854,383 - 116,854,628RGDNCBI36
Celera7111,875,333 - 111,875,578RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,432,775 - 111,433,020UniSTS
CRA_TCAGchr7v27116,462,588 - 116,462,833UniSTS
REN63581  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,066,912 - 117,067,154UniSTSGRCh37
Build 367116,854,148 - 116,854,390RGDNCBI36
Celera7111,875,098 - 111,875,340RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,432,540 - 111,432,782UniSTS
CRA_TCAGchr7v27116,462,353 - 116,462,595UniSTS
REN63582  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,066,685 - 117,066,925UniSTSGRCh37
Build 367116,853,921 - 116,854,161RGDNCBI36
Celera7111,874,871 - 111,875,111RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,432,313 - 111,432,553UniSTS
CRA_TCAGchr7v27116,462,126 - 116,462,366UniSTS
REN63583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,066,463 - 117,066,702UniSTSGRCh37
Build 367116,853,699 - 116,853,938RGDNCBI36
Celera7111,874,649 - 111,874,888RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,432,091 - 111,432,330UniSTS
CRA_TCAGchr7v27116,461,904 - 116,462,143UniSTS
REN63584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,066,172 - 117,066,423UniSTSGRCh37
Build 367116,853,408 - 116,853,659RGDNCBI36
Celera7111,874,358 - 111,874,609RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,431,800 - 111,432,051UniSTS
CRA_TCAGchr7v27116,461,613 - 116,461,864UniSTS
REN63585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,065,904 - 117,066,138UniSTSGRCh37
Build 367116,853,140 - 116,853,374RGDNCBI36
Celera7111,874,090 - 111,874,324RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,431,532 - 111,431,766UniSTS
CRA_TCAGchr7v27116,461,345 - 116,461,579UniSTS
REN63586  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,065,615 - 117,065,842UniSTSGRCh37
Build 367116,852,851 - 116,853,078RGDNCBI36
Celera7111,873,801 - 111,874,028RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,431,243 - 111,431,470UniSTS
CRA_TCAGchr7v27116,461,056 - 116,461,283UniSTS
REN63587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,065,085 - 117,065,317UniSTSGRCh37
Build 367116,852,321 - 116,852,553RGDNCBI36
Celera7111,873,270 - 111,873,502RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,430,712 - 111,430,944UniSTS
HuRef1392,767,180 - 92,767,412UniSTS
CRA_TCAGchr7v27116,460,525 - 116,460,757UniSTS
REN63588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,064,866 - 117,065,100UniSTSGRCh37
Build 367116,852,102 - 116,852,336RGDNCBI36
Celera7111,873,051 - 111,873,285RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,430,493 - 111,430,727UniSTS
CRA_TCAGchr7v27116,460,306 - 116,460,540UniSTS
REN63589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,064,661 - 117,064,885UniSTSGRCh37
Build 367116,851,897 - 116,852,121RGDNCBI36
Celera7111,872,846 - 111,873,070RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,430,288 - 111,430,512UniSTS
CRA_TCAGchr7v27116,460,101 - 116,460,325UniSTS
REN63590  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,064,422 - 117,064,674UniSTSGRCh37
Build 367116,851,658 - 116,851,910RGDNCBI36
Celera7111,872,607 - 111,872,859RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,430,049 - 111,430,301UniSTS
CRA_TCAGchr7v27116,459,862 - 116,460,114UniSTS
REN63591  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,064,195 - 117,064,440UniSTSGRCh37
Build 367116,851,431 - 116,851,676RGDNCBI36
Celera7111,872,380 - 111,872,625RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,429,822 - 111,430,067UniSTS
CRA_TCAGchr7v27116,459,635 - 116,459,880UniSTS
REN63592  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,063,824 - 117,064,071UniSTSGRCh37
Build 367116,851,060 - 116,851,307RGDNCBI36
Celera7111,872,009 - 111,872,256RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,429,451 - 111,429,698UniSTS
CRA_TCAGchr7v27116,459,264 - 116,459,511UniSTS
REN63593  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,063,474 - 117,063,713UniSTSGRCh37
Build 367116,850,710 - 116,850,949RGDNCBI36
Celera7111,871,659 - 111,871,898RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,429,101 - 111,429,340UniSTS
CRA_TCAGchr7v27116,458,914 - 116,459,153UniSTS
REN63594  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,063,184 - 117,063,420UniSTSGRCh37
Build 367116,850,420 - 116,850,656RGDNCBI36
Celera7111,871,369 - 111,871,605RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,428,811 - 111,429,047UniSTS
CRA_TCAGchr7v27116,458,624 - 116,458,860UniSTS
REN63595  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,062,939 - 117,063,169UniSTSGRCh37
Build 367116,850,175 - 116,850,405RGDNCBI36
Celera7111,871,124 - 111,871,354RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,428,566 - 111,428,796UniSTS
CRA_TCAGchr7v27116,458,379 - 116,458,609UniSTS
REN63596  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,062,722 - 117,062,957UniSTSGRCh37
Build 367116,849,958 - 116,850,193RGDNCBI36
Celera7111,870,907 - 111,871,142RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,428,349 - 111,428,584UniSTS
CRA_TCAGchr7v27116,458,162 - 116,458,397UniSTS
REN63597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,062,513 - 117,062,739UniSTSGRCh37
Build 367116,849,749 - 116,849,975RGDNCBI36
Celera7111,870,698 - 111,870,924RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,428,140 - 111,428,366UniSTS
CRA_TCAGchr7v27116,457,953 - 116,458,179UniSTS
REN63598  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,062,236 - 117,062,509UniSTSGRCh37
Build 367116,849,472 - 116,849,745RGDNCBI36
Celera7111,870,421 - 111,870,694RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,427,863 - 111,428,136UniSTS
CRA_TCAGchr7v27116,457,676 - 116,457,949UniSTS
REN63599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,061,956 - 117,062,204UniSTSGRCh37
Build 367116,849,192 - 116,849,440RGDNCBI36
Celera7111,870,141 - 111,870,389RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,427,583 - 111,427,831UniSTS
CRA_TCAGchr7v27116,457,396 - 116,457,644UniSTS
REN63600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,061,711 - 117,061,937UniSTSGRCh37
Build 367116,848,947 - 116,849,173RGDNCBI36
Celera7111,869,896 - 111,870,122RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,427,338 - 111,427,564UniSTS
CRA_TCAGchr7v27116,457,151 - 116,457,377UniSTS
REN63601  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,061,385 - 117,061,647UniSTSGRCh37
Build 367116,848,621 - 116,848,883RGDNCBI36
Celera7111,869,570 - 111,869,832RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,427,012 - 111,427,274UniSTS
CRA_TCAGchr7v27116,456,825 - 116,457,087UniSTS
REN63602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,060,915 - 117,061,174UniSTSGRCh37
Build 367116,848,151 - 116,848,410RGDNCBI36
Celera7111,869,100 - 111,869,359RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,426,542 - 111,426,801UniSTS
CRA_TCAGchr7v27116,456,355 - 116,456,614UniSTS
REN63603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,060,648 - 117,060,894UniSTSGRCh37
Build 367116,847,884 - 116,848,130RGDNCBI36
Celera7111,868,833 - 111,869,079RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,426,275 - 111,426,521UniSTS
CRA_TCAGchr7v27116,456,088 - 116,456,334UniSTS
REN63604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,060,432 - 117,060,658UniSTSGRCh37
Build 367116,847,668 - 116,847,894RGDNCBI36
Celera7111,868,617 - 111,868,843RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,426,059 - 111,426,285UniSTS
CRA_TCAGchr7v27116,455,872 - 116,456,098UniSTS
REN63605  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,060,172 - 117,060,403UniSTSGRCh37
Build 367116,847,408 - 116,847,639RGDNCBI36
Celera7111,868,357 - 111,868,588RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,425,799 - 111,426,030UniSTS
CRA_TCAGchr7v27116,455,612 - 116,455,843UniSTS
REN63606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,059,900 - 117,060,130UniSTSGRCh37
Build 367116,847,136 - 116,847,366RGDNCBI36
Celera7111,868,085 - 111,868,315RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,425,527 - 111,425,757UniSTS
CRA_TCAGchr7v27116,455,340 - 116,455,570UniSTS
REN63607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,059,644 - 117,059,910UniSTSGRCh37
Build 367116,846,880 - 116,847,146RGDNCBI36
Celera7111,867,829 - 111,868,095RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,425,271 - 111,425,537UniSTS
CRA_TCAGchr7v27116,455,084 - 116,455,350UniSTS
REN63608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,059,420 - 117,059,658UniSTSGRCh37
Build 367116,846,656 - 116,846,894RGDNCBI36
Celera7111,867,605 - 111,867,843RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,425,047 - 111,425,285UniSTS
CRA_TCAGchr7v27116,454,860 - 116,455,098UniSTS
REN63609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,059,183 - 117,059,433UniSTSGRCh37
Build 367116,846,419 - 116,846,669RGDNCBI36
Celera7111,867,368 - 111,867,618RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,424,810 - 111,425,060UniSTS
CRA_TCAGchr7v27116,454,623 - 116,454,873UniSTS
REN63610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,058,937 - 117,059,202UniSTSGRCh37
Build 367116,846,173 - 116,846,438RGDNCBI36
Celera7111,867,122 - 111,867,387RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,424,564 - 111,424,829UniSTS
CRA_TCAGchr7v27116,454,377 - 116,454,642UniSTS
REN63611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,058,721 - 117,058,955UniSTSGRCh37
Build 367116,845,957 - 116,846,191RGDNCBI36
Celera7111,866,906 - 111,867,140RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,424,348 - 111,424,582UniSTS
CRA_TCAGchr7v27116,454,161 - 116,454,395UniSTS
REN63612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,058,354 - 117,058,604UniSTSGRCh37
Build 367116,845,590 - 116,845,840RGDNCBI36
Celera7111,866,540 - 111,866,790RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,423,981 - 111,424,231UniSTS
CRA_TCAGchr7v27116,453,796 - 116,454,046UniSTS
REN63613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,058,127 - 117,058,366UniSTSGRCh37
Build 367116,845,363 - 116,845,602RGDNCBI36
Celera7111,866,313 - 111,866,552RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,423,754 - 111,423,993UniSTS
CRA_TCAGchr7v27116,453,569 - 116,453,808UniSTS
REN63614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,057,910 - 117,058,146UniSTSGRCh37
Build 367116,845,146 - 116,845,382RGDNCBI36
Celera7111,866,096 - 111,866,332RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,423,537 - 111,423,773UniSTS
CRA_TCAGchr7v27116,453,352 - 116,453,588UniSTS
REN63615  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,057,685 - 117,057,923UniSTSGRCh37
Build 367116,844,921 - 116,845,159RGDNCBI36
Celera7111,865,871 - 111,866,109RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,423,312 - 111,423,550UniSTS
CRA_TCAGchr7v27116,453,127 - 116,453,365UniSTS
REN63616  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,057,405 - 117,057,641UniSTSGRCh37
Build 367116,844,641 - 116,844,877RGDNCBI36
Celera7111,865,591 - 111,865,827RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,423,032 - 111,423,268UniSTS
CRA_TCAGchr7v27116,452,847 - 116,453,083UniSTS
REN63617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,057,120 - 117,057,359UniSTSGRCh37
Build 367116,844,356 - 116,844,595RGDNCBI36
Celera7111,865,306 - 111,865,545RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,422,747 - 111,422,986UniSTS
CRA_TCAGchr7v27116,452,562 - 116,452,801UniSTS
REN63618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,056,900 - 117,057,131UniSTSGRCh37
Build 367116,844,136 - 116,844,367RGDNCBI36
Celera7111,865,086 - 111,865,317RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,422,527 - 111,422,758UniSTS
CRA_TCAGchr7v27116,452,342 - 116,452,573UniSTS
REN63619  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,056,646 - 117,056,876UniSTSGRCh37
Build 367116,843,882 - 116,844,112RGDNCBI36
Celera7111,864,832 - 111,865,062RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,422,273 - 111,422,503UniSTS
CRA_TCAGchr7v27116,452,088 - 116,452,318UniSTS
REN63620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,056,317 - 117,056,561UniSTSGRCh37
Build 367116,843,553 - 116,843,797RGDNCBI36
Celera7111,864,503 - 111,864,747RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,421,944 - 111,422,188UniSTS
CRA_TCAGchr7v27116,451,759 - 116,452,003UniSTS
REN63621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,056,100 - 117,056,333UniSTSGRCh37
Build 367116,843,336 - 116,843,569RGDNCBI36
Celera7111,864,286 - 111,864,519RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,421,727 - 111,421,960UniSTS
CRA_TCAGchr7v27116,451,542 - 116,451,775UniSTS
REN63622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,055,740 - 117,055,969UniSTSGRCh37
Build 367116,842,976 - 116,843,205RGDNCBI36
Celera7111,863,926 - 111,864,155RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,421,367 - 111,421,596UniSTS
CRA_TCAGchr7v27116,451,182 - 116,451,411UniSTS
REN63623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,055,491 - 117,055,718UniSTSGRCh37
Build 367116,842,727 - 116,842,954RGDNCBI36
Celera7111,863,677 - 111,863,904RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,421,118 - 111,421,345UniSTS
CRA_TCAGchr7v27116,450,933 - 116,451,160UniSTS
REN63624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,055,244 - 117,055,475UniSTSGRCh37
Build 367116,842,480 - 116,842,711RGDNCBI36
Celera7111,863,430 - 111,863,661RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,420,871 - 111,421,102UniSTS
CRA_TCAGchr7v27116,450,686 - 116,450,917UniSTS
REN63625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,054,331 - 117,054,594UniSTSGRCh37
Build 367116,841,567 - 116,841,830RGDNCBI36
Celera7111,862,517 - 111,862,780RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,419,958 - 111,420,221UniSTS
CRA_TCAGchr7v27116,449,773 - 116,450,036UniSTS
REN63626  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,054,034 - 117,054,262UniSTSGRCh37
Build 367116,841,270 - 116,841,498RGDNCBI36
Celera7111,862,220 - 111,862,448RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,419,661 - 111,419,889UniSTS
CRA_TCAGchr7v27116,449,476 - 116,449,704UniSTS
REN63627  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,053,779 - 117,054,051UniSTSGRCh37
Build 367116,841,015 - 116,841,287RGDNCBI36
Celera7111,861,965 - 111,862,237RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,419,406 - 111,419,678UniSTS
CRA_TCAGchr7v27116,449,221 - 116,449,493UniSTS
REN63628  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,053,558 - 117,053,797UniSTSGRCh37
Build 367116,840,794 - 116,841,033RGDNCBI36
Celera7111,861,744 - 111,861,983RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,419,185 - 111,419,424UniSTS
CRA_TCAGchr7v27116,449,000 - 116,449,239UniSTS
REN63629  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,053,275 - 117,053,499UniSTSGRCh37
Build 367116,840,511 - 116,840,735RGDNCBI36
Celera7111,861,461 - 111,861,685RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,418,902 - 111,419,126UniSTS
CRA_TCAGchr7v27116,448,717 - 116,448,941UniSTS
REN63630  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,053,003 - 117,053,263UniSTSGRCh37
Build 367116,840,239 - 116,840,499RGDNCBI36
Celera7111,861,189 - 111,861,449RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,418,630 - 111,418,890UniSTS
CRA_TCAGchr7v27116,448,445 - 116,448,705UniSTS
REN63631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,052,754 - 117,053,007UniSTSGRCh37
Build 367116,839,990 - 116,840,243RGDNCBI36
Celera7111,860,940 - 111,861,193RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,418,381 - 111,418,634UniSTS
CRA_TCAGchr7v27116,448,196 - 116,448,449UniSTS
REN63632  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,052,445 - 117,052,685UniSTSGRCh37
Build 367116,839,681 - 116,839,921RGDNCBI36
Celera7111,860,631 - 111,860,871RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,418,072 - 111,418,312UniSTS
CRA_TCAGchr7v27116,447,887 - 116,448,127UniSTS
REN63633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,052,205 - 117,052,459UniSTSGRCh37
Build 367116,839,441 - 116,839,695RGDNCBI36
Celera7111,860,391 - 111,860,645RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,417,832 - 111,418,086UniSTS
CRA_TCAGchr7v27116,447,647 - 116,447,901UniSTS
REN63634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,051,838 - 117,052,082UniSTSGRCh37
Build 367116,839,074 - 116,839,318RGDNCBI36
Celera7111,860,024 - 111,860,268RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,417,465 - 111,417,709UniSTS
CRA_TCAGchr7v27116,447,280 - 116,447,524UniSTS
REN63635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,051,572 - 117,051,799UniSTSGRCh37
Build 367116,838,808 - 116,839,035RGDNCBI36
Celera7111,859,758 - 111,859,985RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,417,199 - 111,417,426UniSTS
CRA_TCAGchr7v27116,447,014 - 116,447,241UniSTS
REN63636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,051,333 - 117,051,582UniSTSGRCh37
Build 367116,838,569 - 116,838,818RGDNCBI36
Celera7111,859,519 - 111,859,768RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,416,960 - 111,417,209UniSTS
CRA_TCAGchr7v27116,446,775 - 116,447,024UniSTS
REN63637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,051,121 - 117,051,347UniSTSGRCh37
Build 367116,838,357 - 116,838,583RGDNCBI36
Celera7111,859,307 - 111,859,533RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,416,748 - 111,416,974UniSTS
CRA_TCAGchr7v27116,446,563 - 116,446,789UniSTS
REN63638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,050,845 - 117,051,102UniSTSGRCh37
Build 367116,838,081 - 116,838,338RGDNCBI36
Celera7111,859,031 - 111,859,288RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,416,472 - 111,416,729UniSTS
CRA_TCAGchr7v27116,446,287 - 116,446,544UniSTS
REN63639  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,050,543 - 117,050,774UniSTSGRCh37
Build 367116,837,779 - 116,838,010RGDNCBI36
Celera7111,858,729 - 111,858,960RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,416,170 - 111,416,401UniSTS
CRA_TCAGchr7v27116,445,985 - 116,446,216UniSTS
REN63640  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,050,280 - 117,050,526UniSTSGRCh37
Build 367116,837,516 - 116,837,762RGDNCBI36
Celera7111,858,466 - 111,858,712RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,415,907 - 111,416,153UniSTS
CRA_TCAGchr7v27116,445,722 - 116,445,968UniSTS
REN63641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,049,933 - 117,050,181UniSTSGRCh37
Build 367116,837,169 - 116,837,417RGDNCBI36
Celera7111,858,119 - 111,858,367RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,415,560 - 111,415,808UniSTS
CRA_TCAGchr7v27116,445,375 - 116,445,623UniSTS
REN63642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,049,582 - 117,049,820UniSTSGRCh37
Build 367116,836,818 - 116,837,056RGDNCBI36
Celera7111,857,768 - 111,858,006RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,415,209 - 111,415,447UniSTS
CRA_TCAGchr7v27116,445,024 - 116,445,262UniSTS
REN63643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,049,272 - 117,049,497UniSTSGRCh37
Build 367116,836,508 - 116,836,733RGDNCBI36
Celera7111,857,458 - 111,857,683RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,414,899 - 111,415,124UniSTS
CRA_TCAGchr7v27116,444,714 - 116,444,939UniSTS
REN63644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,049,006 - 117,049,240UniSTSGRCh37
Build 367116,836,242 - 116,836,476RGDNCBI36
Celera7111,857,192 - 111,857,426RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,414,633 - 111,414,867UniSTS
CRA_TCAGchr7v27116,444,448 - 116,444,682UniSTS
REN63645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,048,777 - 117,049,025UniSTSGRCh37
Build 367116,836,013 - 116,836,261RGDNCBI36
Celera7111,856,963 - 111,857,211RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,414,404 - 111,414,652UniSTS
CRA_TCAGchr7v27116,444,219 - 116,444,467UniSTS
REN63646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,048,530 - 117,048,777UniSTSGRCh37
Build 367116,835,766 - 116,836,013RGDNCBI36
Celera7111,856,716 - 111,856,963RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,414,157 - 111,414,404UniSTS
CRA_TCAGchr7v27116,443,972 - 116,444,219UniSTS
REN63647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,048,319 - 117,048,547UniSTSGRCh37
Build 367116,835,555 - 116,835,783RGDNCBI36
Celera7111,856,505 - 111,856,733RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,413,946 - 111,414,174UniSTS
CRA_TCAGchr7v27116,443,761 - 116,443,989UniSTS
REN63648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,048,081 - 117,048,331UniSTSGRCh37
Build 367116,835,317 - 116,835,567RGDNCBI36
Celera7111,856,267 - 111,856,517RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,413,708 - 111,413,958UniSTS
CRA_TCAGchr7v27116,443,523 - 116,443,773UniSTS
REN63649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,047,875 - 117,048,100UniSTSGRCh37
Build 367116,835,111 - 116,835,336RGDNCBI36
Celera7111,856,061 - 111,856,286RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,413,502 - 111,413,727UniSTS
CRA_TCAGchr7v27116,443,317 - 116,443,542UniSTS
REN63650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,047,624 - 117,047,885UniSTSGRCh37
Build 367116,834,860 - 116,835,121RGDNCBI36
Celera7111,855,810 - 111,856,071RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,413,251 - 111,413,512UniSTS
CRA_TCAGchr7v27116,443,066 - 116,443,327UniSTS
REN63651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,047,373 - 117,047,642UniSTSGRCh37
Build 367116,834,609 - 116,834,878RGDNCBI36
Celera7111,855,559 - 111,855,828RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,413,000 - 111,413,269UniSTS
CRA_TCAGchr7v27116,442,815 - 116,443,084UniSTS
REN63652  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,047,122 - 117,047,371UniSTSGRCh37
Build 367116,834,358 - 116,834,607RGDNCBI36
Celera7111,855,308 - 111,855,557RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,412,749 - 111,412,998UniSTS
CRA_TCAGchr7v27116,442,564 - 116,442,813UniSTS
REN63653  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,046,896 - 117,047,121UniSTSGRCh37
Build 367116,834,132 - 116,834,357RGDNCBI36
Celera7111,855,082 - 111,855,307RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,412,523 - 111,412,748UniSTS
CRA_TCAGchr7v27116,442,338 - 116,442,563UniSTS
REN63654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,046,588 - 117,046,857UniSTSGRCh37
Build 367116,833,824 - 116,834,093RGDNCBI36
Celera7111,854,774 - 111,855,043RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,412,215 - 111,412,484UniSTS
CRA_TCAGchr7v27116,442,030 - 116,442,299UniSTS
REN63655  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,046,119 - 117,046,357UniSTSGRCh37
Build 367116,833,355 - 116,833,593RGDNCBI36
Celera7111,854,305 - 111,854,543RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,411,746 - 111,411,984UniSTS
CRA_TCAGchr7v27116,441,561 - 116,441,799UniSTS
REN63656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,045,883 - 117,046,129UniSTSGRCh37
Build 367116,833,119 - 116,833,365RGDNCBI36
Celera7111,854,069 - 111,854,315RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,411,510 - 111,411,756UniSTS
CRA_TCAGchr7v27116,441,325 - 116,441,571UniSTS
REN63657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,045,669 - 117,045,901UniSTSGRCh37
Build 367116,832,905 - 116,833,137RGDNCBI36
Celera7111,853,855 - 111,854,087RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,411,296 - 111,411,528UniSTS
CRA_TCAGchr7v27116,441,111 - 116,441,343UniSTS
REN63658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,045,419 - 117,045,652UniSTSGRCh37
Build 367116,832,655 - 116,832,888RGDNCBI36
Celera7111,853,605 - 111,853,838RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,411,046 - 111,411,279UniSTS
CRA_TCAGchr7v27116,440,861 - 116,441,094UniSTS
REN63659  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,045,189 - 117,045,437UniSTSGRCh37
Build 367116,832,425 - 116,832,673RGDNCBI36
Celera7111,853,375 - 111,853,623RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,410,816 - 111,411,064UniSTS
CRA_TCAGchr7v27116,440,631 - 116,440,879UniSTS
REN63660  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,044,965 - 117,045,193UniSTSGRCh37
Build 367116,832,201 - 116,832,429RGDNCBI36
Celera7111,853,151 - 111,853,379RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,410,592 - 111,410,820UniSTS
CRA_TCAGchr7v27116,440,407 - 116,440,635UniSTS
REN63661  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,044,715 - 117,044,939UniSTSGRCh37
Build 367116,831,951 - 116,832,175RGDNCBI36
Celera7111,852,901 - 111,853,125RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,410,342 - 111,410,566UniSTS
CRA_TCAGchr7v27116,440,157 - 116,440,381UniSTS
REN63662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,044,450 - 117,044,691UniSTSGRCh37
Build 367116,831,686 - 116,831,927RGDNCBI36
Celera7111,852,636 - 111,852,877RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,410,077 - 111,410,318UniSTS
CRA_TCAGchr7v27116,439,892 - 116,440,133UniSTS
REN63663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,044,214 - 117,044,469UniSTSGRCh37
Build 367116,831,450 - 116,831,705RGDNCBI36
Celera7111,852,400 - 111,852,655RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,409,841 - 111,410,096UniSTS
CRA_TCAGchr7v27116,439,656 - 116,439,911UniSTS
REN63664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,044,001 - 117,044,232UniSTSGRCh37
Build 367116,831,237 - 116,831,468RGDNCBI36
Celera7111,852,187 - 111,852,418RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,409,628 - 111,409,859UniSTS
CRA_TCAGchr7v27116,439,443 - 116,439,674UniSTS
REN63665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,043,771 - 117,044,015UniSTSGRCh37
Build 367116,831,007 - 116,831,251RGDNCBI36
Celera7111,851,957 - 111,852,201RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,409,398 - 111,409,642UniSTS
CRA_TCAGchr7v27116,439,213 - 116,439,457UniSTS
REN63666  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,043,516 - 117,043,765UniSTSGRCh37
Build 367116,830,752 - 116,831,001RGDNCBI36
Celera7111,851,702 - 111,851,951RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,409,143 - 111,409,392UniSTS
CRA_TCAGchr7v27116,438,958 - 116,439,207UniSTS
REN63667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,043,267 - 117,043,524UniSTSGRCh37
Build 367116,830,503 - 116,830,760RGDNCBI36
Celera7111,851,453 - 111,851,710RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,408,894 - 111,409,151UniSTS
CRA_TCAGchr7v27116,438,709 - 116,438,966UniSTS
REN63668  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,043,061 - 117,043,286UniSTSGRCh37
Build 367116,830,297 - 116,830,522RGDNCBI36
Celera7111,851,247 - 111,851,472RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,408,688 - 111,408,913UniSTS
CRA_TCAGchr7v27116,438,503 - 116,438,728UniSTS
REN63669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,042,831 - 117,043,074UniSTSGRCh37
Build 367116,830,067 - 116,830,310RGDNCBI36
Celera7111,851,013 - 111,851,260RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,408,454 - 111,408,701UniSTS
CRA_TCAGchr7v27116,438,269 - 116,438,516UniSTS
REN63670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,042,573 - 117,042,804UniSTSGRCh37
Build 367116,829,809 - 116,830,040RGDNCBI36
Celera7111,850,755 - 111,850,986RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,408,196 - 111,408,427UniSTS
CRA_TCAGchr7v27116,438,011 - 116,438,242UniSTS
REN63671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,042,305 - 117,042,544UniSTSGRCh37
Build 367116,829,541 - 116,829,780RGDNCBI36
Celera7111,850,487 - 111,850,726RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,407,928 - 111,408,167UniSTS
CRA_TCAGchr7v27116,437,743 - 116,437,982UniSTS
REN63672  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,042,061 - 117,042,289UniSTSGRCh37
Build 367116,829,297 - 116,829,525RGDNCBI36
Celera7111,850,243 - 111,850,471RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,407,684 - 111,407,912UniSTS
CRA_TCAGchr7v27116,437,499 - 116,437,727UniSTS
REN63673  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,041,751 - 117,042,006UniSTSGRCh37
Build 367116,828,987 - 116,829,242RGDNCBI36
Celera7111,849,933 - 111,850,188RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,407,374 - 111,407,629UniSTS
CRA_TCAGchr7v27116,437,189 - 116,437,444UniSTS
REN63674  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,041,525 - 117,041,752UniSTSGRCh37
Build 367116,828,761 - 116,828,988RGDNCBI36
Celera7111,849,707 - 111,849,934RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,407,148 - 111,407,375UniSTS
CRA_TCAGchr7v27116,436,963 - 116,437,190UniSTS
REN63675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,041,191 - 117,041,438UniSTSGRCh37
Build 367116,828,427 - 116,828,674RGDNCBI36
Celera7111,849,373 - 111,849,620RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,406,814 - 111,407,061UniSTS
CRA_TCAGchr7v27116,436,629 - 116,436,876UniSTS
REN63676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,040,966 - 117,041,208UniSTSGRCh37
Build 367116,828,202 - 116,828,444RGDNCBI36
Celera7111,849,148 - 111,849,390RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,406,589 - 111,406,831UniSTS
CRA_TCAGchr7v27116,436,404 - 116,436,646UniSTS
REN63677  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,040,757 - 117,040,984UniSTSGRCh37
Build 367116,827,993 - 116,828,220RGDNCBI36
Celera7111,848,939 - 111,849,166RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,406,380 - 111,406,607UniSTS
CRA_TCAGchr7v27116,436,195 - 116,436,422UniSTS
REN63678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,040,541 - 117,040,766UniSTSGRCh37
Build 367116,827,777 - 116,828,002RGDNCBI36
Celera7111,848,723 - 111,848,948RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,406,164 - 111,406,389UniSTS
CRA_TCAGchr7v27116,435,979 - 116,436,204UniSTS
REN63679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,040,276 - 117,040,531UniSTSGRCh37
Build 367116,827,512 - 116,827,767RGDNCBI36
Celera7111,848,458 - 111,848,713RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,405,899 - 111,406,154UniSTS
CRA_TCAGchr7v27116,435,714 - 116,435,969UniSTS
REN63680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,040,054 - 117,040,289UniSTSGRCh37
Build 367116,827,290 - 116,827,525RGDNCBI36
Celera7111,848,236 - 111,848,471RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,405,677 - 111,405,912UniSTS
CRA_TCAGchr7v27116,435,492 - 116,435,727UniSTS
REN63681  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,039,674 - 117,039,900UniSTSGRCh37
Build 367116,826,910 - 116,827,136RGDNCBI36
Celera7111,847,856 - 111,848,082RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,405,297 - 111,405,523UniSTS
CRA_TCAGchr7v27116,435,112 - 116,435,338UniSTS
REN63682  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,039,403 - 117,039,654UniSTSGRCh37
Build 367116,826,639 - 116,826,890RGDNCBI36
Celera7111,847,585 - 111,847,836RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,405,026 - 111,405,277UniSTS
CRA_TCAGchr7v27116,434,841 - 116,435,092UniSTS
REN63683  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,039,155 - 117,039,395UniSTSGRCh37
Build 367116,826,391 - 116,826,631RGDNCBI36
Celera7111,847,337 - 111,847,577RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,404,778 - 111,405,018UniSTS
CRA_TCAGchr7v27116,434,593 - 116,434,833UniSTS
REN63684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,038,801 - 117,039,045UniSTSGRCh37
Build 367116,826,037 - 116,826,281RGDNCBI36
Celera7111,846,983 - 111,847,227RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,404,424 - 111,404,668UniSTS
CRA_TCAGchr7v27116,434,239 - 116,434,483UniSTS
REN63685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,038,536 - 117,038,796UniSTSGRCh37
Build 367116,825,772 - 116,826,032RGDNCBI36
Celera7111,846,718 - 111,846,978RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,404,159 - 111,404,419UniSTS
CRA_TCAGchr7v27116,433,974 - 116,434,234UniSTS
REN63686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,038,326 - 117,038,550UniSTSGRCh37
Build 367116,825,562 - 116,825,786RGDNCBI36
Celera7111,846,508 - 111,846,732RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,403,949 - 111,404,173UniSTS
CRA_TCAGchr7v27116,433,764 - 116,433,988UniSTS
REN63687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,038,051 - 117,038,299UniSTSGRCh37
Build 367116,825,287 - 116,825,535RGDNCBI36
Celera7111,846,233 - 111,846,481RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,403,674 - 111,403,922UniSTS
CRA_TCAGchr7v27116,433,489 - 116,433,737UniSTS
REN63688  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,037,839 - 117,038,070UniSTSGRCh37
Build 367116,825,075 - 116,825,306RGDNCBI36
Celera7111,846,021 - 111,846,252RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,403,462 - 111,403,693UniSTS
CRA_TCAGchr7v27116,433,277 - 116,433,508UniSTS
REN63689  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,037,615 - 117,037,857UniSTSGRCh37
Build 367116,824,851 - 116,825,093RGDNCBI36
Celera7111,845,797 - 111,846,039RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,403,238 - 111,403,480UniSTS
CRA_TCAGchr7v27116,433,053 - 116,433,295UniSTS
REN63690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,037,370 - 117,037,597UniSTSGRCh37
Build 367116,824,606 - 116,824,833RGDNCBI36
Celera7111,845,552 - 111,845,779RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,402,993 - 111,403,220UniSTS
CRA_TCAGchr7v27116,432,808 - 116,433,035UniSTS
REN63691  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,037,162 - 117,037,386UniSTSGRCh37
Build 367116,824,398 - 116,824,622RGDNCBI36
Celera7111,845,344 - 111,845,568RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,402,785 - 111,403,009UniSTS
CRA_TCAGchr7v27116,432,600 - 116,432,824UniSTS
REN63692  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,036,726 - 117,036,951UniSTSGRCh37
Build 367116,823,962 - 116,824,187RGDNCBI36
Celera7111,844,908 - 111,845,133RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,402,349 - 111,402,574UniSTS
CRA_TCAGchr7v27116,432,164 - 116,432,389UniSTS
REN63693  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,036,389 - 117,036,632UniSTSGRCh37
Build 367116,823,625 - 116,823,868RGDNCBI36
Celera7111,844,571 - 111,844,814RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,402,012 - 111,402,255UniSTS
CRA_TCAGchr7v27116,431,827 - 116,432,070UniSTS
REN63694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,036,069 - 117,036,293UniSTSGRCh37
Build 367116,823,305 - 116,823,529RGDNCBI36
Celera7111,844,251 - 111,844,475RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,401,692 - 111,401,916UniSTS
CRA_TCAGchr7v27116,431,507 - 116,431,731UniSTS
REN63695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,035,847 - 117,036,071UniSTSGRCh37
Build 367116,823,083 - 116,823,307RGDNCBI36
Celera7111,844,029 - 111,844,253RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,401,470 - 111,401,694UniSTS
CRA_TCAGchr7v27116,431,285 - 116,431,509UniSTS
REN63696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,035,541 - 117,035,777UniSTSGRCh37
Build 367116,822,777 - 116,823,013RGDNCBI36
Celera7111,843,723 - 111,843,959RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,401,164 - 111,401,400UniSTS
CRA_TCAGchr7v27116,430,979 - 116,431,215UniSTS
REN63697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,035,323 - 117,035,560UniSTSGRCh37
Build 367116,822,559 - 116,822,796RGDNCBI36
Celera7111,843,505 - 111,843,742RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,400,946 - 111,401,183UniSTS
CRA_TCAGchr7v27116,430,761 - 116,430,998UniSTS
REN63698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,035,068 - 117,035,335UniSTSGRCh37
Build 367116,822,304 - 116,822,571RGDNCBI36
Celera7111,843,250 - 111,843,517RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,400,691 - 111,400,958UniSTS
CRA_TCAGchr7v27116,430,506 - 116,430,773UniSTS
REN63699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,034,849 - 117,035,086UniSTSGRCh37
Build 367116,822,085 - 116,822,322RGDNCBI36
Celera7111,843,031 - 111,843,268RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,400,472 - 111,400,709UniSTS
CRA_TCAGchr7v27116,430,287 - 116,430,524UniSTS
REN63700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,034,626 - 117,034,861UniSTSGRCh37
Build 367116,821,862 - 116,822,097RGDNCBI36
Celera7111,842,808 - 111,843,043RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,400,249 - 111,400,484UniSTS
CRA_TCAGchr7v27116,430,064 - 116,430,299UniSTS
REN63701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,034,395 - 117,034,627UniSTSGRCh37
Build 367116,821,631 - 116,821,863RGDNCBI36
Celera7111,842,577 - 111,842,809RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,400,018 - 111,400,250UniSTS
CRA_TCAGchr7v27116,429,833 - 116,430,065UniSTS
REN63702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,033,773 - 117,033,997UniSTSGRCh37
Build 367116,821,009 - 116,821,233RGDNCBI36
Celera7111,841,955 - 111,842,179RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,399,396 - 111,399,620UniSTS
CRA_TCAGchr7v27116,429,211 - 116,429,435UniSTS
REN63703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,033,547 - 117,033,792UniSTSGRCh37
Build 367116,820,783 - 116,821,028RGDNCBI36
Celera7111,841,729 - 111,841,974RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,399,170 - 111,399,415UniSTS
CRA_TCAGchr7v27116,428,985 - 116,429,230UniSTS
REN63704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,033,252 - 117,033,518UniSTSGRCh37
Build 367116,820,488 - 116,820,754RGDNCBI36
Celera7111,841,434 - 111,841,700RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,398,875 - 111,399,141UniSTS
CRA_TCAGchr7v27116,428,690 - 116,428,956UniSTS
REN63705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,032,512 - 117,032,749UniSTSGRCh37
Build 367116,819,748 - 116,819,985RGDNCBI36
Celera7111,840,694 - 111,840,931RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,398,135 - 111,398,372UniSTS
CRA_TCAGchr7v27116,427,950 - 116,428,187UniSTS
REN63706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,032,080 - 117,032,335UniSTSGRCh37
Build 367116,819,316 - 116,819,571RGDNCBI36
Celera7111,840,262 - 111,840,517RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,397,703 - 111,397,958UniSTS
CRA_TCAGchr7v27116,427,518 - 116,427,773UniSTS
REN63707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,031,689 - 117,031,943UniSTSGRCh37
Build 367116,818,925 - 116,819,179RGDNCBI36
Celera7111,839,871 - 111,840,125RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,397,312 - 111,397,566UniSTS
CRA_TCAGchr7v27116,427,127 - 116,427,381UniSTS
REN63708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,031,427 - 117,031,678UniSTSGRCh37
Build 367116,818,663 - 116,818,914RGDNCBI36
Celera7111,839,609 - 111,839,860RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,397,050 - 111,397,301UniSTS
CRA_TCAGchr7v27116,426,865 - 116,427,116UniSTS
REN63709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,030,974 - 117,031,215UniSTSGRCh37
Build 367116,818,210 - 116,818,451RGDNCBI36
Celera7111,839,156 - 111,839,397RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,396,597 - 111,396,838UniSTS
CRA_TCAGchr7v27116,426,412 - 116,426,653UniSTS
REN63710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,030,516 - 117,030,745UniSTSGRCh37
Build 367116,817,752 - 116,817,981RGDNCBI36
Celera7111,838,698 - 111,838,927RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,396,139 - 111,396,368UniSTS
CRA_TCAGchr7v27116,425,954 - 116,426,183UniSTS
REN63711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,030,243 - 117,030,471UniSTSGRCh37
Build 367116,817,479 - 116,817,707RGDNCBI36
Celera7111,838,425 - 111,838,653RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,395,866 - 111,396,094UniSTS
CRA_TCAGchr7v27116,425,681 - 116,425,909UniSTS
REN63712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,029,993 - 117,030,232UniSTSGRCh37
Build 367116,817,229 - 116,817,468RGDNCBI36
Celera7111,838,175 - 111,838,414RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,395,616 - 111,395,855UniSTS
CRA_TCAGchr7v27116,425,431 - 116,425,670UniSTS
REN63713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,029,766 - 117,029,996UniSTSGRCh37
Build 367116,817,002 - 116,817,232RGDNCBI36
Celera7111,837,948 - 111,838,178RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,395,389 - 111,395,619UniSTS
CRA_TCAGchr7v27116,425,204 - 116,425,434UniSTS
REN63714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,029,501 - 117,029,741UniSTSGRCh37
Build 367116,816,737 - 116,816,977RGDNCBI36
Celera7111,837,683 - 111,837,923RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,395,124 - 111,395,364UniSTS
CRA_TCAGchr7v27116,424,939 - 116,425,179UniSTS
REN63715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,029,247 - 117,029,486UniSTSGRCh37
Build 367116,816,483 - 116,816,722RGDNCBI36
Celera7111,837,429 - 111,837,668RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,394,870 - 111,395,109UniSTS
CRA_TCAGchr7v27116,424,685 - 116,424,924UniSTS
REN63716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,028,968 - 117,029,228UniSTSGRCh37
Build 367116,816,204 - 116,816,464RGDNCBI36
Celera7111,837,150 - 111,837,410RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,394,591 - 111,394,851UniSTS
CRA_TCAGchr7v27116,424,406 - 116,424,666UniSTS
REN63717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,028,728 - 117,028,953UniSTSGRCh37
Build 367116,815,964 - 116,816,189RGDNCBI36
Celera7111,836,910 - 111,837,135RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,394,351 - 111,394,576UniSTS
CRA_TCAGchr7v27116,424,166 - 116,424,391UniSTS
REN63718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,028,494 - 117,028,718UniSTSGRCh37
Build 367116,815,730 - 116,815,954RGDNCBI36
Celera7111,836,676 - 111,836,900RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,394,117 - 111,394,341UniSTS
CRA_TCAGchr7v27116,423,932 - 116,424,156UniSTS
REN63719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,028,157 - 117,028,413UniSTSGRCh37
Build 367116,815,393 - 116,815,649RGDNCBI36
Celera7111,836,339 - 111,836,595RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,393,780 - 111,394,036UniSTS
CRA_TCAGchr7v27116,423,595 - 116,423,851UniSTS
REN63720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,027,935 - 117,028,159UniSTSGRCh37
Build 367116,815,171 - 116,815,395RGDNCBI36
Celera7111,836,117 - 111,836,341RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,393,558 - 111,393,782UniSTS
CRA_TCAGchr7v27116,423,373 - 116,423,597UniSTS
REN63721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,027,643 - 117,027,907UniSTSGRCh37
Build 367116,814,879 - 116,815,143RGDNCBI36
Celera7111,835,825 - 111,836,089RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,393,266 - 111,393,530UniSTS
CRA_TCAGchr7v27116,423,081 - 116,423,345UniSTS
REN63722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,027,419 - 117,027,658UniSTSGRCh37
Build 367116,814,655 - 116,814,894RGDNCBI36
Celera7111,835,601 - 111,835,840RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,393,042 - 111,393,281UniSTS
CRA_TCAGchr7v27116,422,857 - 116,423,096UniSTS
REN63723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,027,174 - 117,027,413UniSTSGRCh37
Build 367116,814,410 - 116,814,649RGDNCBI36
Celera7111,835,356 - 111,835,595RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,392,797 - 111,393,036UniSTS
CRA_TCAGchr7v27116,422,612 - 116,422,851UniSTS
REN63724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,026,791 - 117,027,039UniSTSGRCh37
Build 367116,814,027 - 116,814,275RGDNCBI36
Celera7111,834,973 - 111,835,221RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,392,414 - 111,392,662UniSTS
CRA_TCAGchr7v27116,422,229 - 116,422,477UniSTS
REN63725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,026,498 - 117,026,742UniSTSGRCh37
Build 367116,813,734 - 116,813,978RGDNCBI36
Celera7111,834,680 - 111,834,924RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,392,121 - 111,392,365UniSTS
CRA_TCAGchr7v27116,421,936 - 116,422,180UniSTS
REN63726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,026,261 - 117,026,502UniSTSGRCh37
Build 367116,813,497 - 116,813,738RGDNCBI36
Celera7111,834,443 - 111,834,684RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,391,884 - 111,392,125UniSTS
CRA_TCAGchr7v27116,421,699 - 116,421,940UniSTS
REN63727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,026,017 - 117,026,263UniSTSGRCh37
Build 367116,813,253 - 116,813,499RGDNCBI36
Celera7111,834,199 - 111,834,445RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,391,640 - 111,391,886UniSTS
CRA_TCAGchr7v27116,421,455 - 116,421,701UniSTS
REN63728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,025,809 - 117,026,033UniSTSGRCh37
Build 367116,813,045 - 116,813,269RGDNCBI36
Celera7111,833,991 - 111,834,215RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,391,432 - 111,391,656UniSTS
CRA_TCAGchr7v27116,421,247 - 116,421,471UniSTS
REN63729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,025,591 - 117,025,817UniSTSGRCh37
Build 367116,812,827 - 116,813,053RGDNCBI36
Celera7111,833,773 - 111,833,999RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,391,214 - 111,391,440UniSTS
CRA_TCAGchr7v27116,421,029 - 116,421,255UniSTS
REN63730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,024,881 - 117,025,113UniSTSGRCh37
Build 367116,812,117 - 116,812,349RGDNCBI36
Celera7111,833,063 - 111,833,295RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,390,504 - 111,390,736UniSTS
CRA_TCAGchr7v27116,420,319 - 116,420,551UniSTS
REN63731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,024,625 - 117,024,865UniSTSGRCh37
Build 367116,811,861 - 116,812,101RGDNCBI36
Celera7111,832,807 - 111,833,047RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,390,248 - 111,390,488UniSTS
CRA_TCAGchr7v27116,420,063 - 116,420,303UniSTS
REN63732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,024,412 - 117,024,636UniSTSGRCh37
Build 367116,811,648 - 116,811,872RGDNCBI36
Celera7111,832,594 - 111,832,818RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,390,035 - 111,390,259UniSTS
CRA_TCAGchr7v27116,419,850 - 116,420,074UniSTS
REN63733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,024,075 - 117,024,333UniSTSGRCh37
Build 367116,811,311 - 116,811,569RGDNCBI36
Celera7111,832,257 - 111,832,515RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,389,698 - 111,389,956UniSTS
CRA_TCAGchr7v27116,419,513 - 116,419,771UniSTS
REN63734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,023,805 - 117,024,063UniSTSGRCh37
Build 367116,811,041 - 116,811,299RGDNCBI36
Celera7111,831,987 - 111,832,245RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,389,428 - 111,389,686UniSTS
CRA_TCAGchr7v27116,419,243 - 116,419,501UniSTS
REN63735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,023,543 - 117,023,808UniSTSGRCh37
Build 367116,810,779 - 116,811,044RGDNCBI36
Celera7111,831,725 - 111,831,990RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,389,166 - 111,389,431UniSTS
CRA_TCAGchr7v27116,418,981 - 116,419,246UniSTS
REN63736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,023,234 - 117,023,458UniSTSGRCh37
Build 367116,810,470 - 116,810,694RGDNCBI36
Celera7111,831,416 - 111,831,640RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,388,857 - 111,389,081UniSTS
CRA_TCAGchr7v27116,418,672 - 116,418,896UniSTS
REN63737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,023,002 - 117,023,247UniSTSGRCh37
Build 367116,810,238 - 116,810,483RGDNCBI36
Celera7111,831,184 - 111,831,429RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,388,625 - 111,388,870UniSTS
CRA_TCAGchr7v27116,418,440 - 116,418,685UniSTS
REN63738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,022,359 - 117,022,611UniSTSGRCh37
Build 367116,809,595 - 116,809,847RGDNCBI36
Celera7111,830,541 - 111,830,793RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,387,982 - 111,388,234UniSTS
CRA_TCAGchr7v27116,417,797 - 116,418,049UniSTS
REN63739  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,022,122 - 117,022,346UniSTSGRCh37
Build 367116,809,358 - 116,809,582RGDNCBI36
Celera7111,830,304 - 111,830,528RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,387,745 - 111,387,969UniSTS
CRA_TCAGchr7v27116,417,560 - 116,417,784UniSTS
REN63740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,021,867 - 117,022,099UniSTSGRCh37
Build 367116,809,103 - 116,809,335RGDNCBI36
Celera7111,830,049 - 111,830,281RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,387,490 - 111,387,722UniSTS
CRA_TCAGchr7v27116,417,305 - 116,417,537UniSTS
REN63741  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,021,646 - 117,021,881UniSTSGRCh37
Build 367116,808,882 - 116,809,117RGDNCBI36
Celera7111,829,828 - 111,830,063RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,387,269 - 111,387,504UniSTS
CRA_TCAGchr7v27116,417,084 - 116,417,319UniSTS
REN63742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,021,433 - 117,021,657UniSTSGRCh37
Build 367116,808,669 - 116,808,893RGDNCBI36
Celera7111,829,615 - 111,829,839RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,387,056 - 111,387,280UniSTS
CRA_TCAGchr7v27116,416,871 - 116,417,095UniSTS
REN63743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,021,182 - 117,021,412UniSTSGRCh37
Build 367116,808,418 - 116,808,648RGDNCBI36
Celera7111,829,364 - 111,829,594RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,386,805 - 111,387,035UniSTS
CRA_TCAGchr7v27116,416,620 - 116,416,850UniSTS
REN63744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,020,922 - 117,021,193UniSTSGRCh37
Build 367116,808,158 - 116,808,429RGDNCBI36
Celera7111,829,104 - 111,829,375RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,386,545 - 111,386,816UniSTS
CRA_TCAGchr7v27116,416,360 - 116,416,631UniSTS
REN63745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,020,689 - 117,020,928UniSTSGRCh37
Build 367116,807,925 - 116,808,164RGDNCBI36
Celera7111,828,871 - 111,829,110RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,386,312 - 111,386,551UniSTS
CRA_TCAGchr7v27116,416,127 - 116,416,366UniSTS
REN63746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,020,342 - 117,020,602UniSTSGRCh37
Build 367116,807,578 - 116,807,838RGDNCBI36
Celera7111,828,524 - 111,828,784RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,385,965 - 111,386,225UniSTS
CRA_TCAGchr7v27116,415,780 - 116,416,040UniSTS
REN63747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,020,082 - 117,020,353UniSTSGRCh37
Build 367116,807,318 - 116,807,589RGDNCBI36
Celera7111,828,264 - 111,828,535RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,385,705 - 111,385,976UniSTS
CRA_TCAGchr7v27116,415,520 - 116,415,791UniSTS
REN63748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,019,780 - 117,020,014UniSTSGRCh37
Build 367116,807,016 - 116,807,250RGDNCBI36
Celera7111,827,962 - 111,828,196RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,385,403 - 111,385,637UniSTS
CRA_TCAGchr7v27116,415,218 - 116,415,452UniSTS
REN63749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,019,519 - 117,019,743UniSTSGRCh37
Build 367116,806,755 - 116,806,979RGDNCBI36
Celera7111,827,701 - 111,827,925RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,385,142 - 111,385,366UniSTS
CRA_TCAGchr7v27116,414,957 - 116,415,181UniSTS
REN63750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,019,298 - 117,019,538UniSTSGRCh37
Build 367116,806,534 - 116,806,774RGDNCBI36
Celera7111,827,480 - 111,827,720RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,384,921 - 111,385,161UniSTS
CRA_TCAGchr7v27116,414,736 - 116,414,976UniSTS
REN63751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,019,080 - 117,019,317UniSTSGRCh37
Build 367116,806,316 - 116,806,553RGDNCBI36
Celera7111,827,262 - 111,827,499RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,384,703 - 111,384,940UniSTS
CRA_TCAGchr7v27116,414,518 - 116,414,755UniSTS
REN63752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,018,829 - 117,019,086UniSTSGRCh37
Build 367116,806,065 - 116,806,322RGDNCBI36
Celera7111,827,011 - 111,827,268RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,384,452 - 111,384,709UniSTS
CRA_TCAGchr7v27116,414,267 - 116,414,524UniSTS
REN63753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,018,576 - 117,018,807UniSTSGRCh37
Build 367116,805,812 - 116,806,043RGDNCBI36
Celera7111,826,758 - 111,826,989RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,384,199 - 111,384,430UniSTS
CRA_TCAGchr7v27116,414,014 - 116,414,245UniSTS
REN63754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,018,337 - 117,018,564UniSTSGRCh37
Build 367116,805,573 - 116,805,800RGDNCBI36
Celera7111,826,519 - 111,826,746RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,383,960 - 111,384,187UniSTS
CRA_TCAGchr7v27116,413,775 - 116,414,002UniSTS
REN63755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,018,049 - 117,018,290UniSTSGRCh37
Build 367116,805,285 - 116,805,526RGDNCBI36
Celera7111,826,231 - 111,826,472RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,383,672 - 111,383,913UniSTS
CRA_TCAGchr7v27116,413,487 - 116,413,728UniSTS
REN63756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,017,814 - 117,018,045UniSTSGRCh37
Build 367116,805,050 - 116,805,281RGDNCBI36
Celera7111,825,996 - 111,826,227RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,383,437 - 111,383,668UniSTS
CRA_TCAGchr7v27116,413,252 - 116,413,483UniSTS
REN63757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,017,537 - 117,017,807UniSTSGRCh37
Build 367116,804,773 - 116,805,043RGDNCBI36
Celera7111,825,719 - 111,825,989RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,383,160 - 111,383,430UniSTS
CRA_TCAGchr7v27116,412,975 - 116,413,245UniSTS
REN63758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,017,279 - 117,017,551UniSTSGRCh37
Build 367116,804,515 - 116,804,787RGDNCBI36
Celera7111,825,461 - 111,825,733RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,382,902 - 111,383,174UniSTS
CRA_TCAGchr7v27116,412,717 - 116,412,989UniSTS
REN63759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,016,908 - 117,017,151UniSTSGRCh37
Build 367116,804,144 - 116,804,387RGDNCBI36
Celera7111,825,090 - 111,825,333RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,382,531 - 111,382,774UniSTS
CRA_TCAGchr7v27116,412,346 - 116,412,589UniSTS
REN63760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,016,698 - 117,016,922UniSTSGRCh37
Build 367116,803,934 - 116,804,158RGDNCBI36
Celera7111,824,880 - 111,825,104RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,382,321 - 111,382,545UniSTS
CRA_TCAGchr7v27116,412,136 - 116,412,360UniSTS
REN63761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,016,396 - 117,016,660UniSTSGRCh37
Build 367116,803,632 - 116,803,896RGDNCBI36
Celera7111,824,578 - 111,824,842RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,382,019 - 111,382,283UniSTS
CRA_TCAGchr7v27116,411,834 - 116,412,098UniSTS
REN63762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,016,152 - 117,016,398UniSTSGRCh37
Build 367116,803,388 - 116,803,634RGDNCBI36
Celera7111,824,334 - 111,824,580RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,381,775 - 111,382,021UniSTS
CRA_TCAGchr7v27116,411,590 - 116,411,836UniSTS
REN63763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,015,860 - 117,016,128UniSTSGRCh37
Build 367116,803,096 - 116,803,364RGDNCBI36
Celera7111,824,042 - 111,824,310RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,381,483 - 111,381,751UniSTS
CRA_TCAGchr7v27116,411,298 - 116,411,566UniSTS
REN63764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,015,620 - 117,015,852UniSTSGRCh37
Build 367116,802,856 - 116,803,088RGDNCBI36
Celera7111,823,802 - 111,824,034RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,381,243 - 111,381,475UniSTS
CRA_TCAGchr7v27116,411,058 - 116,411,290UniSTS
REN63765  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,015,374 - 117,015,598UniSTSGRCh37
Build 367116,802,610 - 116,802,834RGDNCBI36
Celera7111,823,556 - 111,823,780RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,380,997 - 111,381,221UniSTS
CRA_TCAGchr7v27116,410,812 - 116,411,036UniSTS
REN63766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,015,011 - 117,015,254UniSTSGRCh37
Build 367116,802,247 - 116,802,490RGDNCBI36
Celera7111,823,193 - 111,823,436RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,380,634 - 111,380,877UniSTS
CRA_TCAGchr7v27116,410,449 - 116,410,692UniSTS
REN63767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,014,802 - 117,015,026UniSTSGRCh37
Build 367116,802,038 - 116,802,262RGDNCBI36
Celera7111,822,984 - 111,823,208RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,380,425 - 111,380,649UniSTS
CRA_TCAGchr7v27116,410,240 - 116,410,464UniSTS
REN63768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,014,241 - 117,014,466UniSTSGRCh37
Build 367116,801,477 - 116,801,702RGDNCBI36
Celera7111,822,423 - 111,822,648RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,379,864 - 111,380,089UniSTS
CRA_TCAGchr7v27116,409,679 - 116,409,904UniSTS
REN63769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,013,901 - 117,014,139UniSTSGRCh37
Build 367116,801,137 - 116,801,375RGDNCBI36
Celera7111,822,083 - 111,822,321RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,379,524 - 111,379,762UniSTS
CRA_TCAGchr7v27116,409,339 - 116,409,577UniSTS
REN63770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,013,653 - 117,013,891UniSTSGRCh37
Build 367116,800,889 - 116,801,127RGDNCBI36
Celera7111,821,835 - 111,822,073RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,379,276 - 111,379,514UniSTS
CRA_TCAGchr7v27116,409,091 - 116,409,329UniSTS
REN63771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,013,417 - 117,013,643UniSTSGRCh37
Build 367116,800,653 - 116,800,879RGDNCBI36
Celera7111,821,599 - 111,821,825RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,379,040 - 111,379,266UniSTS
CRA_TCAGchr7v27116,408,855 - 116,409,081UniSTS
REN63772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,013,039 - 117,013,295UniSTSGRCh37
Build 367116,800,275 - 116,800,531RGDNCBI36
Celera7111,821,221 - 111,821,477RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,378,662 - 111,378,918UniSTS
CRA_TCAGchr7v27116,408,477 - 116,408,733UniSTS
REN63773  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,012,781 - 117,013,033UniSTSGRCh37
Build 367116,800,017 - 116,800,269RGDNCBI36
Celera7111,820,963 - 111,821,215RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,378,404 - 111,378,656UniSTS
CRA_TCAGchr7v27116,408,219 - 116,408,471UniSTS
REN63774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,012,555 - 117,012,799UniSTSGRCh37
Build 367116,799,791 - 116,800,035RGDNCBI36
Celera7111,820,737 - 111,820,981RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,378,178 - 111,378,422UniSTS
CRA_TCAGchr7v27116,407,993 - 116,408,237UniSTS
REN63775  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,012,341 - 117,012,569UniSTSGRCh37
Build 367116,799,577 - 116,799,805RGDNCBI36
Celera7111,820,523 - 111,820,751RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,377,964 - 111,378,192UniSTS
CRA_TCAGchr7v27116,407,779 - 116,408,007UniSTS
REN63776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,012,100 - 117,012,348UniSTSGRCh37
Build 367116,799,336 - 116,799,584RGDNCBI36
Celera7111,820,282 - 111,820,530RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,377,723 - 111,377,971UniSTS
CRA_TCAGchr7v27116,407,538 - 116,407,786UniSTS
REN63777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,011,883 - 117,012,117UniSTSGRCh37
Build 367116,799,119 - 116,799,353RGDNCBI36
Celera7111,820,065 - 111,820,299RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,377,506 - 111,377,740UniSTS
CRA_TCAGchr7v27116,407,321 - 116,407,555UniSTS
REN63778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,011,645 - 117,011,887UniSTSGRCh37
Build 367116,798,881 - 116,799,123RGDNCBI36
Celera7111,819,827 - 111,820,069RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,377,268 - 111,377,510UniSTS
CRA_TCAGchr7v27116,407,083 - 116,407,325UniSTS
REN63779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,011,295 - 117,011,524UniSTSGRCh37
Build 367116,798,531 - 116,798,760RGDNCBI36
Celera7111,819,477 - 111,819,706RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,376,918 - 111,377,147UniSTS
CRA_TCAGchr7v27116,406,733 - 116,406,962UniSTS
REN63780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,010,947 - 117,011,203UniSTSGRCh37
Build 367116,798,183 - 116,798,439RGDNCBI36
Celera7111,819,129 - 111,819,385RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,376,570 - 111,376,826UniSTS
CRA_TCAGchr7v27116,406,385 - 116,406,641UniSTS
REN63781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,010,701 - 117,010,963UniSTSGRCh37
Build 367116,797,937 - 116,798,199RGDNCBI36
Celera7111,818,883 - 111,819,145RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,376,324 - 111,376,586UniSTS
CRA_TCAGchr7v27116,406,139 - 116,406,401UniSTS
REN63782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,010,488 - 117,010,719UniSTSGRCh37
Build 367116,797,724 - 116,797,955RGDNCBI36
Celera7111,818,670 - 111,818,901RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,376,111 - 111,376,342UniSTS
CRA_TCAGchr7v27116,405,926 - 116,406,157UniSTS
REN63783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,010,267 - 117,010,502UniSTSGRCh37
Build 367116,797,503 - 116,797,738RGDNCBI36
Celera7111,818,449 - 111,818,684RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,375,890 - 111,376,125UniSTS
CRA_TCAGchr7v27116,405,705 - 116,405,940UniSTS
REN63784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,010,038 - 117,010,270UniSTSGRCh37
Build 367116,797,274 - 116,797,506RGDNCBI36
Celera7111,818,220 - 111,818,452RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,375,661 - 111,375,893UniSTS
CRA_TCAGchr7v27116,405,476 - 116,405,708UniSTS
REN63785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,009,771 - 117,010,015UniSTSGRCh37
Build 367116,797,007 - 116,797,251RGDNCBI36
Celera7111,817,953 - 111,818,197RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,375,394 - 111,375,638UniSTS
CRA_TCAGchr7v27116,405,209 - 116,405,453UniSTS
REN63786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,009,529 - 117,009,763UniSTSGRCh37
Build 367116,796,765 - 116,796,999RGDNCBI36
Celera7111,817,711 - 111,817,945RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,375,152 - 111,375,386UniSTS
CRA_TCAGchr7v27116,404,967 - 116,405,201UniSTS
REN63787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,009,278 - 117,009,510UniSTSGRCh37
Build 367116,796,514 - 116,796,746RGDNCBI36
Celera7111,817,460 - 111,817,692RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,374,901 - 111,375,133UniSTS
CRA_TCAGchr7v27116,404,716 - 116,404,948UniSTS
REN63788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,009,023 - 117,009,275UniSTSGRCh37
Build 367116,796,259 - 116,796,511RGDNCBI36
Celera7111,817,205 - 111,817,457RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,374,646 - 111,374,898UniSTS
CRA_TCAGchr7v27116,404,461 - 116,404,713UniSTS
REN63789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,008,814 - 117,009,041UniSTSGRCh37
Build 367116,796,050 - 116,796,277RGDNCBI36
Celera7111,816,996 - 111,817,223RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,374,437 - 111,374,664UniSTS
CRA_TCAGchr7v27116,404,252 - 116,404,479UniSTS
REN63790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,008,599 - 117,008,823UniSTSGRCh37
Build 367116,795,835 - 116,796,059RGDNCBI36
Celera7111,816,781 - 111,817,005RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,374,222 - 111,374,446UniSTS
CRA_TCAGchr7v27116,404,037 - 116,404,261UniSTS
REN63791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,008,352 - 117,008,579UniSTSGRCh37
Build 367116,795,588 - 116,795,815RGDNCBI36
Celera7111,816,534 - 111,816,761RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,373,975 - 111,374,202UniSTS
CRA_TCAGchr7v27116,403,790 - 116,404,017UniSTS
REN63792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,008,095 - 117,008,369UniSTSGRCh37
Build 367116,795,331 - 116,795,605RGDNCBI36
Celera7111,816,277 - 111,816,551RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,373,718 - 111,373,992UniSTS
CRA_TCAGchr7v27116,403,533 - 116,403,807UniSTS
REN63793  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,007,688 - 117,007,914UniSTSGRCh37
Build 367116,794,924 - 116,795,150RGDNCBI36
Celera7111,815,870 - 111,816,096RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,373,311 - 111,373,537UniSTS
CRA_TCAGchr7v27116,403,126 - 116,403,352UniSTS
REN63794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,007,312 - 117,007,562UniSTSGRCh37
Build 367116,794,548 - 116,794,798RGDNCBI36
Celera7111,815,494 - 111,815,744RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,372,935 - 111,373,185UniSTS
CRA_TCAGchr7v27116,402,750 - 116,403,000UniSTS
REN63795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,007,097 - 117,007,327UniSTSGRCh37
Build 367116,794,333 - 116,794,563RGDNCBI36
Celera7111,815,279 - 111,815,509RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,372,720 - 111,372,950UniSTS
CRA_TCAGchr7v27116,402,535 - 116,402,765UniSTS
REN63796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,006,830 - 117,007,097UniSTSGRCh37
Build 367116,794,066 - 116,794,333RGDNCBI36
Celera7111,815,012 - 111,815,279RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,372,453 - 111,372,720UniSTS
CRA_TCAGchr7v27116,402,268 - 116,402,535UniSTS
REN63797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,006,605 - 117,006,837UniSTSGRCh37
Build 367116,793,841 - 116,794,073RGDNCBI36
Celera7111,814,787 - 111,815,019RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,372,228 - 111,372,460UniSTS
CRA_TCAGchr7v27116,402,043 - 116,402,275UniSTS
REN63798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,006,335 - 117,006,588UniSTSGRCh37
Build 367116,793,571 - 116,793,824RGDNCBI36
Celera7111,814,517 - 111,814,770RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,371,958 - 111,372,211UniSTS
CRA_TCAGchr7v27116,401,773 - 116,402,026UniSTS
REN63799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,005,805 - 117,006,038UniSTSGRCh37
Build 367116,793,041 - 116,793,274RGDNCBI36
Celera7111,813,987 - 111,814,220RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,371,428 - 111,371,661UniSTS
CRA_TCAGchr7v27116,401,243 - 116,401,476UniSTS
REN63800  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,005,581 - 117,005,816UniSTSGRCh37
Build 367116,792,817 - 116,793,052RGDNCBI36
Celera7111,813,763 - 111,813,998RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,371,204 - 111,371,439UniSTS
CRA_TCAGchr7v27116,401,019 - 116,401,254UniSTS
REN63801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,005,360 - 117,005,592UniSTSGRCh37
Build 367116,792,596 - 116,792,828RGDNCBI36
Celera7111,813,542 - 111,813,774RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,370,983 - 111,371,215UniSTS
CRA_TCAGchr7v27116,400,798 - 116,401,030UniSTS
REN63802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,005,112 - 117,005,352UniSTSGRCh37
Build 367116,792,348 - 116,792,588RGDNCBI36
Celera7111,813,294 - 111,813,534RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,370,735 - 111,370,975UniSTS
CRA_TCAGchr7v27116,400,550 - 116,400,790UniSTS
REN63803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,004,822 - 117,005,046UniSTSGRCh37
Build 367116,792,058 - 116,792,282RGDNCBI36
Celera7111,813,004 - 111,813,228RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,370,445 - 111,370,669UniSTS
CRA_TCAGchr7v27116,400,260 - 116,400,484UniSTS
REN63804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,004,581 - 117,004,833UniSTSGRCh37
Build 367116,791,817 - 116,792,069RGDNCBI36
Celera7111,812,763 - 111,813,015RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,370,204 - 111,370,456UniSTS
CRA_TCAGchr7v27116,400,019 - 116,400,271UniSTS
REN63805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,004,358 - 117,004,598UniSTSGRCh37
Build 367116,791,594 - 116,791,834RGDNCBI36
Celera7111,812,540 - 111,812,780RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,369,981 - 111,370,221UniSTS
CRA_TCAGchr7v27116,399,796 - 116,400,036UniSTS
REN63806  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,004,127 - 117,004,351UniSTSGRCh37
Build 367116,791,363 - 116,791,587RGDNCBI36
Celera7111,812,309 - 111,812,533RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,369,750 - 111,369,974UniSTS
CRA_TCAGchr7v27116,399,565 - 116,399,789UniSTS
REN63807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,003,777 - 117,004,001UniSTSGRCh37
Build 367116,791,013 - 116,791,237RGDNCBI36
Celera7111,811,959 - 111,812,183RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,369,400 - 111,369,624UniSTS
CRA_TCAGchr7v27116,399,215 - 116,399,439UniSTS
REN63808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,003,572 - 117,003,796UniSTSGRCh37
Build 367116,790,808 - 116,791,032RGDNCBI36
Celera7111,811,754 - 111,811,978RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,369,195 - 111,369,419UniSTS
CRA_TCAGchr7v27116,399,010 - 116,399,234UniSTS
REN63809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,003,327 - 117,003,565UniSTSGRCh37
Build 367116,790,563 - 116,790,801RGDNCBI36
Celera7111,811,509 - 111,811,747RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,368,950 - 111,369,188UniSTS
CRA_TCAGchr7v27116,398,765 - 116,399,003UniSTS
REN63810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,002,976 - 117,003,202UniSTSGRCh37
Build 367116,790,212 - 116,790,438RGDNCBI36
Celera7111,811,158 - 111,811,384RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,368,599 - 111,368,825UniSTS
CRA_TCAGchr7v27116,398,414 - 116,398,640UniSTS
stSG598599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,003,320 - 117,003,676UniSTSGRCh37
Build 367116,790,556 - 116,790,912RGDNCBI36
Celera7111,811,502 - 111,811,858RGD
Cytogenetic Map7q31.2UniSTS
HuRef7111,368,943 - 111,369,299UniSTS
CRA_TCAGchr7v27116,398,758 - 116,399,114UniSTS
stSG598600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,003,683 - 117,004,800UniSTSGRCh37
Build 367116,790,919 - 116,792,036RGDNCBI36
Celera7111,811,865 - 111,812,982RGD
HuRef7111,369,306 - 111,370,423UniSTS
CRA_TCAGchr7v27116,399,121 - 116,400,238UniSTS
stSG598601  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,004,782 - 117,005,793UniSTSGRCh37
Build 367116,792,018 - 116,793,029RGDNCBI36
Celera7111,812,964 - 111,813,975RGD
HuRef7111,370,405 - 111,371,416UniSTS
CRA_TCAGchr7v27116,400,220 - 116,401,231UniSTS
stSG598602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,005,774 - 117,007,119UniSTSGRCh37
Build 367116,793,010 - 116,794,355RGDNCBI36
Celera7111,813,956 - 111,815,301RGD
HuRef7111,371,397 - 111,372,742UniSTS
CRA_TCAGchr7v27116,401,212 - 116,402,557UniSTS
stSG598603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,007,100 - 117,008,377UniSTSGRCh37
Build 367116,794,336 - 116,795,613RGDNCBI36
Celera7111,815,282 - 111,816,559RGD
HuRef7111,372,723 - 111,374,000UniSTS
CRA_TCAGchr7v27116,402,538 - 116,403,815UniSTS
stSG598604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,008,363 - 117,009,849UniSTSGRCh37
Build 367116,795,599 - 116,797,085RGDNCBI36
Celera7111,816,545 - 111,818,031RGD
HuRef7111,373,986 - 111,375,472UniSTS
CRA_TCAGchr7v27116,403,801 - 116,405,287UniSTS
stSG598605  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,009,830 - 117,011,301UniSTSGRCh37
Build 367116,797,066 - 116,798,537RGDNCBI36
Celera7111,818,012 - 111,819,483RGD
HuRef7111,375,453 - 111,376,924UniSTS
CRA_TCAGchr7v27116,405,268 - 116,406,739UniSTS
stSG598606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,011,287 - 117,012,650UniSTSGRCh37
Build 367116,798,523 - 116,799,886RGDNCBI36
Celera7111,819,469 - 111,820,832RGD
HuRef7111,376,910 - 111,378,273UniSTS
CRA_TCAGchr7v27116,406,725 - 116,408,088UniSTS
stSG598607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,012,632 - 117,013,877UniSTSGRCh37
Build 367116,799,868 - 116,801,113RGDNCBI36
Celera7111,820,814 - 111,822,059RGD
HuRef7111,378,255 - 111,379,500UniSTS
CRA_TCAGchr7v27116,408,070 - 116,409,315UniSTS
stSG598608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,013,868 - 117,015,104UniSTSGRCh37
Build 367116,801,104 - 116,802,340RGDNCBI36
Celera7111,822,050 - 111,823,286RGD
HuRef7111,379,491 - 111,380,727UniSTS
CRA_TCAGchr7v27116,409,306 - 116,410,542UniSTS
stSG598609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,015,085 - 117,015,285UniSTSGRCh37
Build 367116,802,321 - 116,802,521RGDNCBI36
Celera7111,823,267 - 111,823,467RGD
HuRef7111,380,708 - 111,380,908UniSTS
CRA_TCAGchr7v27116,410,523 - 116,410,723UniSTS
stSG598610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,019,700 - 117,020,721UniSTSGRCh37
Build 367116,806,936 - 116,807,957RGDNCBI36
Celera7111,827,882 - 111,828,903RGD
HuRef7111,385,323 - 111,386,344UniSTS
CRA_TCAGchr7v27116,415,138 - 116,416,159UniSTS
stSG598611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,020,711 - 117,021,905UniSTSGRCh37
Build 367116,807,947 - 116,809,141RGDNCBI36
Celera7111,828,893 - 111,830,087RGD
HuRef7111,386,334 - 111,387,528UniSTS
CRA_TCAGchr7v27116,416,149 - 116,417,343UniSTS
stSG598612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,021,885 - 117,023,130UniSTSGRCh37
Build 367116,809,121 - 116,810,366RGDNCBI36
Celera7111,830,067 - 111,831,312RGD
HuRef7111,387,508 - 111,388,753UniSTS
CRA_TCAGchr7v27116,417,323 - 116,418,568UniSTS
stSG598613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,023,110 - 117,024,115UniSTSGRCh37
Build 367116,810,346 - 116,811,351RGDNCBI36
Celera7111,831,292 - 111,832,297RGD
HuRef7111,388,733 - 111,389,738UniSTS
CRA_TCAGchr7v27116,418,548 - 116,419,553UniSTS
stSG598614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,024,096 - 117,025,114UniSTSGRCh37
Build 367116,811,332 - 116,812,350RGDNCBI36
Celera7111,832,278 - 111,833,296RGD
HuRef7111,389,719 - 111,390,737UniSTS
CRA_TCAGchr7v27116,419,534 - 116,420,552UniSTS
stSG598615  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,025,172 - 117,026,570UniSTSGRCh37
Build 367116,812,408 - 116,813,806RGDNCBI36
Celera7111,833,354 - 111,834,752RGD
HuRef7111,390,795 - 111,392,193UniSTS
CRA_TCAGchr7v27116,420,610 - 116,422,008UniSTS
stSG598616  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,026,633 - 117,027,848UniSTSGRCh37
Build 367116,813,869 - 116,815,084RGDNCBI36
Celera7111,834,815 - 111,836,030RGD
HuRef7111,392,256 - 111,393,471UniSTS
CRA_TCAGchr7v27116,422,071 - 116,423,286UniSTS
stSG598617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,027,842 - 117,029,179UniSTSGRCh37
Build 367116,815,078 - 116,816,415RGDNCBI36
Celera7111,836,024 - 111,837,361RGD
HuRef7111,393,465 - 111,394,802UniSTS
CRA_TCAGchr7v27116,423,280 - 116,424,617UniSTS
stSG598618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,032,787 - 117,033,929UniSTSGRCh37
Build 367116,820,023 - 116,821,165RGDNCBI36
Celera7111,840,969 - 111,842,111RGD
HuRef7111,398,410 - 111,399,552UniSTS
CRA_TCAGchr7v27116,428,225 - 116,429,367UniSTS
stSG598619  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,033,910 - 117,034,091UniSTSGRCh37
Build 367116,821,146 - 116,821,327RGDNCBI36
Celera7111,842,092 - 111,842,273RGD
HuRef7111,399,533 - 111,399,714UniSTS
CRA_TCAGchr7v27116,429,348 - 116,429,529UniSTS
stSG598620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,034,143 - 117,035,342UniSTSGRCh37
Build 367116,821,379 - 116,822,578RGDNCBI36
Celera7111,842,325 - 111,843,524RGD
HuRef7111,399,766 - 111,400,965UniSTS
CRA_TCAGchr7v27116,429,581 - 116,430,780UniSTS
stSG598621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,035,068 - 117,036,071UniSTSGRCh37
Build 367116,822,304 - 116,823,307RGDNCBI36
Celera7111,843,250 - 111,844,253RGD
HuRef7111,400,691 - 111,401,694UniSTS
CRA_TCAGchr7v27116,430,506 - 116,431,509UniSTS
stSG598622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,036,050 - 117,037,395UniSTSGRCh37
Build 367116,823,286 - 116,824,631RGDNCBI36
Celera7111,844,232 - 111,845,577RGD
HuRef7111,401,673 - 111,403,018UniSTS
CRA_TCAGchr7v27116,431,488 - 116,432,833UniSTS
stSG598623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,037,379 - 117,038,683UniSTSGRCh37
Build 367116,824,615 - 116,825,919RGDNCBI36
Celera7111,845,561 - 111,846,865RGD
HuRef7111,403,002 - 111,404,306UniSTS
CRA_TCAGchr7v27116,432,817 - 116,434,121UniSTS
stSG598624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,038,791 - 117,040,085UniSTSGRCh37
Build 367116,826,027 - 116,827,321RGDNCBI36
Celera7111,846,973 - 111,848,267RGD
HuRef7111,404,414 - 111,405,708UniSTS
CRA_TCAGchr7v27116,434,229 - 116,435,523UniSTS
stSG598625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,040,066 - 117,041,082UniSTSGRCh37
Build 367116,827,302 - 116,828,318RGDNCBI36
Celera7111,848,248 - 111,849,264RGD
HuRef7111,405,689 - 111,406,705UniSTS
CRA_TCAGchr7v27116,435,504 - 116,436,520UniSTS
stSG598628  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,050,194 - 117,051,241UniSTSGRCh37
Build 367116,837,430 - 116,838,477RGDNCBI36
Celera7111,858,380 - 111,859,427RGD
HuRef7111,415,821 - 111,416,868UniSTS
CRA_TCAGchr7v27116,445,636 - 116,446,683UniSTS
stSG598629  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,051,222 - 117,052,238UniSTSGRCh37
Build 367116,838,458 - 116,839,474RGDNCBI36
Celera7111,859,408 - 111,860,424RGD
HuRef7111,416,849 - 111,417,865UniSTS
CRA_TCAGchr7v27116,446,664 - 116,447,680UniSTS
stSG598631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,053,283 - 117,054,399UniSTSGRCh37
Build 367116,840,519 - 116,841,635RGDNCBI36
Celera7111,861,469 - 111,862,585RGD
HuRef7111,418,910 - 111,420,026UniSTS
CRA_TCAGchr7v27116,448,725 - 116,449,841UniSTS
stSG598632  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,054,380 - 117,055,879UniSTSGRCh37
Build 367116,841,616 - 116,843,115RGDNCBI36
Celera7111,862,566 - 111,864,065RGD
HuRef7111,420,007 - 111,421,506UniSTS
CRA_TCAGchr7v27116,449,822 - 116,451,321UniSTS
stSG598633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,055,877 - 117,057,354UniSTSGRCh37
Build 367116,843,113 - 116,844,590RGDNCBI36
Celera7111,864,063 - 111,865,540RGD
HuRef7111,421,504 - 111,422,981UniSTS
CRA_TCAGchr7v27116,451,319 - 116,452,796UniSTS
stSG598634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,057,335 - 117,058,363UniSTSGRCh37
Build 367116,844,571 - 116,845,599RGDNCBI36
Celera7111,865,521 - 111,866,549RGD
HuRef7111,422,962 - 111,423,990UniSTS
CRA_TCAGchr7v27116,452,777 - 116,453,805UniSTS
stSG598635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,058,342 - 117,059,664UniSTSGRCh37
Build 367116,845,578 - 116,846,900RGDNCBI36
Celera7111,866,528 - 111,867,849RGD
HuRef7111,423,969 - 111,425,291UniSTS
CRA_TCAGchr7v27116,453,784 - 116,455,104UniSTS
stSG598636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,059,645 - 117,060,860UniSTSGRCh37
Build 367116,846,881 - 116,848,096RGDNCBI36
Celera7111,867,830 - 111,869,045RGD
HuRef7111,425,272 - 111,426,487UniSTS
CRA_TCAGchr7v27116,455,085 - 116,456,300UniSTS
stSG598637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,060,841 - 117,062,329UniSTSGRCh37
Build 367116,848,077 - 116,849,565RGDNCBI36
Celera7111,869,026 - 111,870,514RGD
HuRef7111,426,468 - 111,427,956UniSTS
CRA_TCAGchr7v27116,456,281 - 116,457,769UniSTS
stSG598638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,062,310 - 117,063,347UniSTSGRCh37
Build 367116,849,546 - 116,850,583RGDNCBI36
Celera7111,870,495 - 111,871,532RGD
HuRef7111,427,937 - 111,428,974UniSTS
CRA_TCAGchr7v27116,457,750 - 116,458,787UniSTS
stSG598639  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,063,331 - 117,064,482UniSTSGRCh37
Build 367116,850,567 - 116,851,718RGDNCBI36
Celera7111,871,516 - 111,872,667RGD
HuRef7111,428,958 - 111,430,109UniSTS
CRA_TCAGchr7v27116,458,771 - 116,459,922UniSTS
stSG598640  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,064,465 - 117,065,721UniSTSGRCh37
Build 367116,851,701 - 116,852,957RGDNCBI36
Celera7111,872,650 - 111,873,907RGD
HuRef7111,430,092 - 111,431,349UniSTS
CRA_TCAGchr7v27116,459,905 - 116,461,162UniSTS
stSG598641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,065,708 - 117,067,182UniSTSGRCh37
Build 367116,852,944 - 116,854,418RGDNCBI36
Celera7111,873,894 - 111,875,368RGD
HuRef7111,431,336 - 111,432,810UniSTS
CRA_TCAGchr7v27116,461,149 - 116,462,623UniSTS
stSG598642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,067,170 - 117,068,386UniSTSGRCh37
Build 367116,854,406 - 116,855,622RGDNCBI36
Celera7111,875,356 - 111,876,572RGD
HuRef7111,432,798 - 111,434,014UniSTS
CRA_TCAGchr7v27116,462,611 - 116,463,827UniSTS
stSG598643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377117,068,302 - 117,069,304UniSTSGRCh37
Build 367116,855,538 - 116,856,540RGDNCBI36
Celera7111,876,488 - 111,877,490RGD
HuRef7111,433,930 - 111,434,932UniSTS
CRA_TCAGchr7v27116,463,743 - 116,464,745UniSTS


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 adipose tissue appendage
High
Medium 1 11 1 368
Low 6 8 5 8 5 4 4 1 7 30 64 3
Below cutoff 238 218 217 45 173 30 397 187 274 66 268 666 16 111 240

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001301821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001301822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_130768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC002465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF461259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC028695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC034963 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC068488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC098399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC126186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC126188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144212 (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
  DB457846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HC006784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HC044669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000284629   ⟹   ENSP00000284629
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7117,363,222 - 117,427,493 (-)Ensembl
RefSeq Acc Id: ENST00000428663   ⟹   ENSP00000402919
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7117,422,272 - 117,428,123 (-)Ensembl
RefSeq Acc Id: ENST00000450714   ⟹   ENSP00000389791
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7117,363,536 - 117,427,507 (-)Ensembl
RefSeq Acc Id: ENST00000463182
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7117,363,308 - 117,427,498 (-)Ensembl
RefSeq Acc Id: ENST00000465832
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7117,363,315 - 117,427,505 (-)Ensembl
RefSeq Acc Id: ENST00000479454
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7117,363,308 - 117,427,503 (-)Ensembl
RefSeq Acc Id: NM_001301821   ⟹   NP_001288750
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387117,363,222 - 117,427,493 (-)NCBI
CHM1_17116,936,638 - 117,000,932 (-)NCBI
T2T-CHM13v2.07118,678,562 - 118,742,828 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001301822   ⟹   NP_001288751
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387117,363,222 - 117,427,493 (-)NCBI
CHM1_17116,936,638 - 117,000,932 (-)NCBI
T2T-CHM13v2.07118,678,562 - 118,742,828 (-)NCBI
Sequence:
RefSeq Acc Id: NM_130768   ⟹   NP_570124
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387117,363,222 - 117,427,493 (-)NCBI
GRCh377117,003,276 - 117,067,577 (-)RGD
Build 367116,790,512 - 116,854,779 (-)NCBI Archive
Celera7111,811,458 - 111,875,763 (-)RGD
HuRef7111,368,899 - 111,433,205 (-)ENTREZGENE
CHM1_17116,936,638 - 117,000,932 (-)NCBI
T2T-CHM13v2.07118,678,562 - 118,742,828 (-)NCBI
CRA_TCAGchr7v27116,398,714 - 116,463,018 (-)ENTREZGENE
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_570124   ⟸   NM_130768
- Peptide Label: isoform 1
- UniProtKB: A4D0V0 (UniProtKB/Swiss-Prot),   A0AV27 (UniProtKB/Swiss-Prot),   B7ZM20 (UniProtKB/Swiss-Prot),   Q8WWH4 (UniProtKB/Swiss-Prot),   Q49AP3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001288751   ⟸   NM_001301822
- Peptide Label: isoform 3
- UniProtKB: Q8WWH4 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001288750   ⟸   NM_001301821
- Peptide Label: isoform 2
- UniProtKB: Q49AP3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000389791   ⟸   ENST00000450714
RefSeq Acc Id: ENSP00000402919   ⟸   ENST00000428663
RefSeq Acc Id: ENSP00000284629   ⟸   ENST00000284629
Protein Domains
SAM

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8WWH4-F1-model_v2 AlphaFold Q8WWH4 1-475 view protein structure

Promoters
RGD ID:7211767
Promoter ID:EPDNEW_H11628
Type:initiation region
Name:ASZ1_2
Description:ankyrin repeat, SAM and basic leucine zipper domain containing1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11629  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387117,427,505 - 117,427,565EPDNEW
RGD ID:7211765
Promoter ID:EPDNEW_H11629
Type:multiple initiation site
Name:ASZ1_1
Description:ankyrin repeat, SAM and basic leucine zipper domain containing1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11628  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387117,427,619 - 117,427,679EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1350 AgrOrtholog
COSMIC ASZ1 COSMIC
Ensembl Genes ENSG00000154438 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000284629 ENTREZGENE
  ENST00000284629.7 UniProtKB/Swiss-Prot
  ENST00000428663.1 UniProtKB/TrEMBL
  ENST00000450714.2 UniProtKB/TrEMBL
Gene3D-CATH 1.10.150.50 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.25.40.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000154438 GTEx
HGNC ID HGNC:1350 ENTREZGENE
Human Proteome Map ASZ1 Human Proteome Map
InterPro Ankyrin_rpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ankyrin_rpt-contain_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Asz1_SAM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SAM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SAM/pointed_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:136991 UniProtKB/Swiss-Prot
NCBI Gene 136991 ENTREZGENE
OMIM 605797 OMIM
PANTHER ANKYRIN REPEAT, SAM AND BASIC LEUCINE ZIPPER DOMAIN-CONTAINING PROTEIN 1 UniProtKB/Swiss-Prot
  ANKYRIN REPEAT, SAM AND BASIC LEUCINE ZIPPER DOMAIN-CONTAINING PROTEIN 1 UniProtKB/Swiss-Prot
  ANKYRIN REPEAT, SAM AND BASIC LEUCINE ZIPPER DOMAIN-CONTAINING PROTEIN 1 UniProtKB/TrEMBL
  ANKYRIN REPEAT, SAM AND BASIC LEUCINE ZIPPER DOMAIN-CONTAINING PROTEIN 1 UniProtKB/TrEMBL
Pfam Ank UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ank_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ank_4 UniProtKB/TrEMBL
  SAM_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25950 PharmGKB
PRINTS ANKYRIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE ANK_REP_REGION UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ANK_REPEAT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ANK UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Pseudo ankyrin repeat-like UniProtKB/Swiss-Prot
  SSF47769 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48403 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0AV27 ENTREZGENE
  A4D0V0 ENTREZGENE
  ASZ1_HUMAN UniProtKB/Swiss-Prot
  B7ZM20 ENTREZGENE
  C9JP59_HUMAN UniProtKB/TrEMBL
  F8WDQ2_HUMAN UniProtKB/TrEMBL
  Q49AP3 ENTREZGENE, UniProtKB/TrEMBL
  Q8WWH4 ENTREZGENE
UniProt Secondary A0AV27 UniProtKB/Swiss-Prot
  A4D0V0 UniProtKB/Swiss-Prot
  B7ZM20 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-22 ASZ1  ankyrin repeat, SAM and basic leucine zipper domain containing 1  ANKL1  ankyrin-like 1  Data merged from RGD:1353837 737654 PROVISIONAL