MIR100HG (mir-100-let-7a-2-mir-125b-1 cluster host gene)

Gene: MIR100HG (mir-100-let-7a-2-mir-125b-1 cluster host gene) Homo sapiens

Analyze

Symbol:

MIR100HG

Name:

mir-100-let-7a-2-mir-125b-1 cluster host gene

RGD ID:

4892400

HGNC Page

HGNC:39522

Description:

This gene produces long non-coding RNAs that act as regulators of cell proliferation. Alternative promoter usage and splicing results in multiple transcript variants. Some transcript variants may promote growth, while others may act to negatively regulate cell division. [provided by RefSeq, May 2016]

Type:

ncrna (Ensembl: lncRNA)

RefSeq Status:

REVIEWED

Previously known as:

AGD1; DKFZp686J24156; DKFZp686L0115; FLJ11490; FLJ18351; FLJ34394; FLJ41953; linc-NeD125; lncRNA-N2; mir-100-let-7a-2 cluster host gene; RP11-166D19.1

RGD Orthologs

Mouse

Alliance Genes

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	122,028,329 - 122,422,871 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	122,028,325 - 122,556,721 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	121,899,037 - 122,293,579 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Celera	11	119,120,491 - 119,234,460 (-)	NCBI		Celera
Cytogenetic Map	11	q24.1	NCBI
HuRef	11	117,906,349 - 118,020,269 (-)	NCBI		HuRef
CHM1_1	11	121,847,113 - 121,961,069 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	122,057,374 - 122,452,245 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

pulmonary fibrosis (EXP)

schizophrenia (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

4,4'-sulfonyldiphenol (ISO)

acrolein (EXP)

aflatoxin B1 (EXP)

Aflatoxin B2 alpha (EXP)

alpha-pinene (EXP)

arsenous acid (ISO)

benzo[a]pyrene (EXP)

benzo[e]pyrene (EXP)

bisphenol A (EXP,ISO)

bisphenol F (EXP,ISO)

bleomycin A2 (ISO)

calcitriol (EXP)

cisplatin (EXP)

dexamethasone (EXP)

diarsenic trioxide (ISO)

dorsomorphin (EXP)

doxorubicin (EXP)

fipronil (EXP)

formaldehyde (EXP)

fulvestrant (EXP)

methapyrilene (EXP)

methylmercury chloride (EXP)

N,N-diethyl-m-toluamide (EXP)

ozone (EXP)

paracetamol (EXP)

perfluorohexanesulfonic acid (ISO)

phenylmercury acetate (EXP)

propofol (EXP)

SB 431542 (EXP)

triptonide (ISO)

valproic acid (EXP)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Schizophrenia (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:12477932	PMID:14702039	PMID:16344560	PMID:19531736	PMID:19779542	PMID:21031016	PMID:25027842	PMID:26480000	PMID:29748571	PMID:29880533	PMID:30042378	PMID:30102375
PMID:30551532	PMID:30886062	PMID:31619268	PMID:32513696	PMID:35247921	PMID:35279145	PMID:37487022

Genomics

Comparative Map Data

MIR100HG
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	122,028,329 - 122,422,871 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	122,028,325 - 122,556,721 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	121,899,037 - 122,293,579 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Celera	11	119,120,491 - 119,234,460 (-)	NCBI		Celera
Cytogenetic Map	11	q24.1	NCBI
HuRef	11	117,906,349 - 118,020,269 (-)	NCBI		HuRef
CHM1_1	11	121,847,113 - 121,961,069 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	122,057,374 - 122,452,245 (-)	NCBI		T2T-CHM13v2.0

Mir100hg
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	9	41,287,822 - 41,526,481 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	9	41,238,373 - 41,628,290 (+)	Ensembl		GRCm39 Ensembl
GRCm38	9	41,376,526 - 41,615,185 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	9	41,327,077 - 41,716,994 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	9	41,389,422 - 41,400,570 (+)	RGD	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	9	41,389,336 - 41,420,847 (+)	RGD		MGSCv36	mm8
Celera	9	38,607,554 - 38,664,028 (+)	NCBI		Celera
Cytogenetic Map	9	A5.1	NCBI
cM Map	9	23.32	NCBI

Variants

Variants in MIR100HG
41 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NR_024430.1(MIR100HG):n.444+20564G>C	single nucleotide variant	Lung cancer [RCV000109683]	Chr11:122134987 [GRCh38] Chr11:122005695 [GRCh37] Chr11:11q24.1	uncertain significance
NR_024430.1(MIR100HG):n.299+3669A>G	single nucleotide variant	Lung cancer [RCV000109684]	Chr11:122199095 [GRCh38] Chr11:122069803 [GRCh37] Chr11:11q24.1	uncertain significance
GRCh38/hg38 11q23.3-24.2(chr11:120426093-124771213)x1	copy number loss	See cases [RCV000134405]	Chr11:120426093..124771213 [GRCh38] Chr11:120296802..124641109 [GRCh37] Chr11:119802012..124146319 [NCBI36] Chr11:11q23.3-24.2	pathogenic
GRCh38/hg38 11q23.3-25(chr11:116851372-134998526)x3	copy number gain	See cases [RCV000134064]	Chr11:116851372..134998526 [GRCh38] Chr11:116722088..134868420 [GRCh37] Chr11:116227298..134373630 [NCBI36] Chr11:11q23.3-25	pathogenic
GRCh38/hg38 11q24.1-24.2(chr11:122182443-125957977)x1	copy number loss	See cases [RCV000136594]	Chr11:122182443..125957977 [GRCh38] Chr11:122053151..125827872 [GRCh37] Chr11:121558361..125333082 [NCBI36] Chr11:11q24.1-24.2	pathogenic
GRCh38/hg38 11q23.2-25(chr11:112864326-131189315)x3	copy number gain	See cases [RCV000137582]	Chr11:112864326..131189315 [GRCh38] Chr11:112832130..131059210 [GRCh37] Chr11:112240259..130564420 [NCBI36] Chr11:11q23.2-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:116868935-135075271)x3	copy number gain	See cases [RCV000137453]	Chr11:116868935..135075271 [GRCh38] Chr11:116739651..134945165 [GRCh37] Chr11:116244861..134450377 [NCBI36] Chr11:11q23.3-25	pathogenic\|conflicting data from submitters
GRCh38/hg38 11q24.1-25(chr11:121780459-135075271)x1	copy number loss	See cases [RCV000138014]	Chr11:121780459..135075271 [GRCh38] Chr11:121651167..134945165 [GRCh37] Chr11:121156377..134450377 [NCBI36] Chr11:11q24.1-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:120515759-135075271)x1	copy number loss	See cases [RCV000138373]	Chr11:120515759..135075271 [GRCh38] Chr11:120386468..134945165 [GRCh37] Chr11:119891678..134450377 [NCBI36] Chr11:11q23.3-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:116806268-135075271)x3	copy number gain	See cases [RCV000138307]	Chr11:116806268..135075271 [GRCh38] Chr11:116676984..134945165 [GRCh37] Chr11:116182194..134450377 [NCBI36] Chr11:11q23.3-25	pathogenic
GRCh38/hg38 11q23.3-24.2(chr11:117333952-127709156)x3	copy number gain	See cases [RCV000139362]	Chr11:117333952..127709156 [GRCh38] Chr11:117204668..127579051 [GRCh37] Chr11:116709878..127084261 [NCBI36] Chr11:11q23.3-24.2	pathogenic
GRCh38/hg38 11q23.3-25(chr11:119424297-135075271)x1	copy number loss	See cases [RCV000138947]	Chr11:119424297..135075271 [GRCh38] Chr11:119295007..134945165 [GRCh37] Chr11:118800217..134450377 [NCBI36] Chr11:11q23.3-25	pathogenic\|likely benign
GRCh38/hg38 11q23.3-24.2(chr11:120080142-125829106)x1	copy number loss	See cases [RCV000140070]	Chr11:120080142..125829106 [GRCh38] Chr11:119950851..125699001 [GRCh37] Chr11:119456061..125204211 [NCBI36] Chr11:11q23.3-24.2	pathogenic
GRCh38/hg38 11q24.1-25(chr11:121689052-135075271)x1	copy number loss	See cases [RCV000139622]	Chr11:121689052..135075271 [GRCh38] Chr11:121559760..134945165 [GRCh37] Chr11:121064970..134450377 [NCBI36] Chr11:11q24.1-25	pathogenic\|likely benign
GRCh38/hg38 11q24.1-25(chr11:121806547-135068576)x1	copy number loss	See cases [RCV000142210]	Chr11:121806547..135068576 [GRCh38] Chr11:121677255..134938470 [GRCh37] Chr11:121182465..134443680 [NCBI36] Chr11:11q24.1-25	pathogenic
GRCh38/hg38 11q24.1-25(chr11:121611476-135068576)x1	copy number loss	See cases [RCV000142185]	Chr11:121611476..135068576 [GRCh38] Chr11:121482185..134938470 [GRCh37] Chr11:120987395..134443680 [NCBI36] Chr11:11q24.1-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3	copy number gain	See cases [RCV000148276]	Chr11:116851395..134998513 [GRCh38] Chr11:116722111..134868407 [GRCh37] Chr11:116227321..134373617 [NCBI36] Chr11:11q23.3-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:118789765-134998513)x3	copy number gain	See cases [RCV000051213]	Chr11:118789765..134998513 [GRCh38] Chr11:118660474..134868407 [GRCh37] Chr11:118165684..134373617 [NCBI36] Chr11:11q23.3-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:119433909-134998513)x1	copy number loss	See cases [RCV000050905]	Chr11:119433909..134998513 [GRCh38] Chr11:119304619..134868407 [GRCh37] Chr11:118809829..134373617 [NCBI36] Chr11:11q23.3-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3	copy number gain	See cases [RCV000050331]	Chr11:116851395..134998513 [GRCh38] Chr11:116722111..134868407 [GRCh37] Chr11:116227321..134373617 [NCBI36] Chr11:11q23.3-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:119215032-134998654)x1	copy number loss	See cases [RCV000052715]	Chr11:119215032..134998654 [GRCh38] Chr11:119085742..134868548 [GRCh37] Chr11:118590952..134373758 [NCBI36] Chr11:11q23.3-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:120507265-134576266)x1	copy number loss	See cases [RCV000052716]	Chr11:120507265..134576266 [GRCh38] Chr11:120377974..134446160 [GRCh37] Chr11:119883184..133951370 [NCBI36] Chr11:11q23.3-25	pathogenic
GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3	copy number gain	See cases [RCV000053638]	Chr11:100348599..135040246 [GRCh38] Chr11:100219331..134910140 [GRCh37] Chr11:99724541..134415350 [NCBI36] Chr11:11q22.1-25	pathogenic
GRCh38/hg38 11q23.3-25(chr11:120236432-135040246)x3	copy number gain	See cases [RCV000053643]	Chr11:120236432..135040246 [GRCh38] Chr11:120107141..134910140 [GRCh37] Chr11:119612351..134415350 [NCBI36] Chr11:11q23.3-25	pathogenic
Single allele	duplication	Schizophrenia [RCV000754124]	Chr11:118989374..135076622 [GRCh38] Chr11:11q23.3-25	likely pathogenic
NM_001001786.3(BLID):c.301T>C (p.Cys101Arg)	single nucleotide variant	Inborn genetic diseases [RCV003245108]	Chr11:122115622 [GRCh38] Chr11:121986330 [GRCh37] Chr11:11q24.1	uncertain significance
Single allele	duplication	not provided [RCV002227754]	Chr11:122413116..123669322 [GRCh38] Chr11:11q24.1	uncertain significance
NM_001001786.3(BLID):c.146C>T (p.Ala49Val)	single nucleotide variant	Inborn genetic diseases [RCV003012774]	Chr11:122115777 [GRCh38] Chr11:121986485 [GRCh37] Chr11:11q24.1	uncertain significance
NM_001001786.3(BLID):c.92G>A (p.Arg31Gln)	single nucleotide variant	Inborn genetic diseases [RCV002729621]	Chr11:122115831 [GRCh38] Chr11:121986539 [GRCh37] Chr11:11q24.1	uncertain significance
NM_001001786.3(BLID):c.36A>G (p.Ile12Met)	single nucleotide variant	Inborn genetic diseases [RCV002897838]	Chr11:122115887 [GRCh38] Chr11:121986595 [GRCh37] Chr11:11q24.1	uncertain significance
NM_001001786.3(BLID):c.37C>T (p.His13Tyr)	single nucleotide variant	Inborn genetic diseases [RCV002965903]	Chr11:122115886 [GRCh38] Chr11:121986594 [GRCh37] Chr11:11q24.1	uncertain significance
NM_001001786.3(BLID):c.230T>G (p.Met77Arg)	single nucleotide variant	Inborn genetic diseases [RCV002714582]	Chr11:122115693 [GRCh38] Chr11:121986401 [GRCh37] Chr11:11q24.1	uncertain significance
NM_001001786.3(BLID):c.131G>A (p.Arg44His)	single nucleotide variant	Inborn genetic diseases [RCV003008593]	Chr11:122115792 [GRCh38] Chr11:121986500 [GRCh37] Chr11:11q24.1	uncertain significance
NM_001001786.3(BLID):c.251A>C (p.His84Pro)	single nucleotide variant	Inborn genetic diseases [RCV003201662]	Chr11:122115672 [GRCh38] Chr11:121986380 [GRCh37] Chr11:11q24.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1513
Count of miRNA genes:	827
Interacting mature miRNAs:	970
Transcripts:	ENST00000524376, ENST00000528986, ENST00000529823, ENST00000530072, ENST00000530955, ENST00000531071, ENST00000531381, ENST00000531470, ENST00000531629, ENST00000532315, ENST00000532319, ENST00000532890, ENST00000534195, ENST00000534297
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

A009L12

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	122,052,612 - 122,052,741	UniSTS	GRCh37
Build 36	11	121,557,822 - 121,557,951	RGD	NCBI36
Celera	11	119,213,290 - 119,213,419	RGD
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	117,999,122 - 117,999,251	UniSTS
GeneMap99-GB4 RH Map	11	401.67	UniSTS
NCBI RH Map	11	1024.0	UniSTS

RH103872

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	121,966,667 - 121,966,796	UniSTS	GRCh37
Build 36	11	121,471,877 - 121,472,006	RGD	NCBI36
Celera	11	119,127,346 - 119,127,475	RGD
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	117,913,205 - 117,913,334	UniSTS
GeneMap99-GB4 RH Map	11	401.67	UniSTS

RH119888

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	122,062,037 - 122,062,307	UniSTS	GRCh37
Build 36	11	121,567,247 - 121,567,517	RGD	NCBI36
Celera	11	119,222,714 - 119,222,994	RGD
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	118,008,545 - 118,008,825	UniSTS
TNG Radiation Hybrid Map	11	58059.0	UniSTS

D11S1860

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	121,968,516 - 121,968,610	UniSTS	GRCh37
Build 36	11	121,473,726 - 121,473,820	RGD	NCBI36
Celera	11	119,129,195 - 119,129,289	RGD
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	117,915,054 - 117,915,148	UniSTS

RH36606

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	122,052,567 - 122,052,761	UniSTS	GRCh37
Build 36	11	121,557,777 - 121,557,971	RGD	NCBI36
Celera	11	119,213,245 - 119,213,439	RGD
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	117,999,077 - 117,999,271	UniSTS
GeneMap99-GB4 RH Map	11	403.56	UniSTS

RH66266

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	122,011,042 - 122,011,180	UniSTS	GRCh37
Build 36	11	121,516,252 - 121,516,390	RGD	NCBI36
Celera	11	119,171,717 - 119,171,855	RGD
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	117,957,574 - 117,957,712	UniSTS
GeneMap99-GB4 RH Map	11	401.6	UniSTS

WI-16084

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	121,959,832 - 121,959,978	UniSTS	GRCh37
Build 36	11	121,465,042 - 121,465,188	RGD	NCBI36
Celera	11	119,120,512 - 119,120,658	RGD
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	117,906,370 - 117,906,516	UniSTS
GeneMap99-GB4 RH Map	11	403.56	UniSTS
Whitehead-RH Map	11	565.0	UniSTS

FB17D4

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	122,011,035 - 122,011,184	UniSTS	GRCh37
Build 36	11	121,516,245 - 121,516,394	RGD	NCBI36
Celera	11	119,171,710 - 119,171,859	RGD
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	117,957,567 - 117,957,716	UniSTS
GeneMap99-GB4 RH Map	11	402.2	UniSTS
Whitehead-RH Map	11	561.4	UniSTS
Whitehead-YAC Contig Map	11		UniSTS

SHGC-31166

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	121,969,063 - 121,969,190	UniSTS	GRCh37
Build 36	11	121,474,273 - 121,474,400	RGD	NCBI36
Celera	11	119,129,742 - 119,129,869	RGD
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	117,915,601 - 117,915,728	UniSTS
GeneMap99-GB4 RH Map	11	401.6	UniSTS
Whitehead-RH Map	11	557.4	UniSTS
GeneMap99-G3 RH Map	11	5517.0	UniSTS

G32641

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	122,052,612 - 122,052,741	UniSTS	GRCh37
Celera	11	119,213,290 - 119,213,419	UniSTS
Cytogenetic Map	11	q24.1	UniSTS
HuRef	11	117,999,122 - 117,999,251	UniSTS

Expression

RNA-SEQ Expression

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

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

High

Medium

1577

1560

984

1492

924

1955

820

965

329

1301

Low

699

667

609

478

476

328

2740

1221

1775

305

582

566

160

875

1452

Below cutoff

725

123

122

775

123

122

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NR_024430	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137175	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137176	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137177	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137178	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137179	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137180	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137181	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137182	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137183	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137184	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137185	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137186	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137187	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137188	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137189	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137190	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137191	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137192	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137193	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137194	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137195	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_137196	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB075498	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB485963	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK021552	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK091713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK123947	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK311309	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK311733	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL832469	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP000755	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP001359	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP001835	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP001924	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC040599	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC089451	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX538058	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX647608	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA027094	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA153922	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA349788	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA474693	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA532588	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA597554	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA649890	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA650430	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA659486	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA769636	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA788103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA808613	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA861327	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB248200	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459770	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459772	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459773	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459774	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459775	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459776	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459777	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459778	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459779	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF459784	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986022	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986023	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986024	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986025	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986026	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986027	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986028	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986029	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986030	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986031	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA986032	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000524376

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,103 - 122,100,448 (-)	Ensembl

RefSeq Acc Id:

ENST00000526674

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,292,274 - 122,422,871 (-)	Ensembl

RefSeq Acc Id:

ENST00000527474

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,180,338 - 122,367,973 (-)	Ensembl

RefSeq Acc Id:

ENST00000528381

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,234,262 - 122,367,815 (-)	Ensembl

RefSeq Acc Id:

ENST00000528986

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,123 - 122,101,686 (-)	Ensembl

RefSeq Acc Id:

ENST00000529733

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,203,509 - 122,367,872 (-)	Ensembl

RefSeq Acc Id:

ENST00000529804

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,858 - 122,309,487 (-)	Ensembl

RefSeq Acc Id:

ENST00000529823

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,103 - 122,102,166 (-)	Ensembl

RefSeq Acc Id:

ENST00000530072

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,103 - 122,101,687 (-)	Ensembl

RefSeq Acc Id:

ENST00000530955

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,327 - 122,101,702 (-)	Ensembl

RefSeq Acc Id:

ENST00000531071

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,123 - 122,102,194 (-)	Ensembl

RefSeq Acc Id:

ENST00000531381

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,103 - 122,102,178 (-)	Ensembl

RefSeq Acc Id:

ENST00000531470

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,378 - 122,070,156 (-)	Ensembl

RefSeq Acc Id:

ENST00000531629

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,100,909 - 122,101,686 (-)	Ensembl

RefSeq Acc Id:

ENST00000532315

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,091,417 - 122,105,942 (-)	Ensembl

RefSeq Acc Id:

ENST00000532319

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,366 - 122,100,492 (-)	Ensembl

RefSeq Acc Id:

ENST00000532350

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,154,200 - 122,203,087 (-)	Ensembl

RefSeq Acc Id:

ENST00000532890

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,117 - 122,101,783 (-)	Ensembl

RefSeq Acc Id:

ENST00000533109

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,154,755 - 122,556,721 (-)	Ensembl

RefSeq Acc Id:

ENST00000534195

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,091,254 - 122,105,169 (-)	Ensembl

RefSeq Acc Id:

ENST00000534297

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,091,545 - 122,180,438 (-)	Ensembl

RefSeq Acc Id:

ENST00000534782

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,091,613 - 122,203,087 (-)	Ensembl

RefSeq Acc Id:

ENST00000636654

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,330 - 122,100,448 (-)	Ensembl

RefSeq Acc Id:

ENST00000637700

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,090,139 - 122,453,731 (-)	Ensembl

RefSeq Acc Id:

ENST00000647591

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,351 - 122,100,475 (-)	Ensembl

RefSeq Acc Id:

ENST00000647749

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,364 - 122,101,697 (-)	Ensembl

RefSeq Acc Id:

ENST00000647967

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,199,119 - 122,203,003 (-)	Ensembl

RefSeq Acc Id:

ENST00000648082

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,854 - 122,422,756 (-)	Ensembl

RefSeq Acc Id:

ENST00000648084

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,233,244 - 122,367,658 (-)	Ensembl

RefSeq Acc Id:

ENST00000648163

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,333 - 122,039,534 (-)	Ensembl

RefSeq Acc Id:

ENST00000648209

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,186 - 122,157,113 (-)	Ensembl

RefSeq Acc Id:

ENST00000648213

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,361 - 122,069,648 (-)	Ensembl

RefSeq Acc Id:

ENST00000648576

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,412,431 - 122,422,839 (-)	Ensembl

RefSeq Acc Id:

ENST00000648734

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,196 - 122,309,451 (-)	Ensembl

RefSeq Acc Id:

ENST00000649216

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,121 - 122,367,977 (-)	Ensembl

RefSeq Acc Id:

ENST00000649293

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,196 - 122,367,605 (-)	Ensembl

RefSeq Acc Id:

ENST00000649544

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,371 - 122,100,539 (-)	Ensembl

RefSeq Acc Id:

ENST00000649626

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,062,395 - 122,101,713 (-)	Ensembl

RefSeq Acc Id:

ENST00000650497

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,144 - 122,156,371 (-)	Ensembl

RefSeq Acc Id:

ENST00000653167

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,230 - 122,105,406 (-)	Ensembl

RefSeq Acc Id:

ENST00000653565

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,338 - 122,203,046 (-)	Ensembl

RefSeq Acc Id:

ENST00000654519

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,111 - 122,102,194 (-)	Ensembl

RefSeq Acc Id:

ENST00000654571

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,174,246 - 122,309,451 (-)	Ensembl

RefSeq Acc Id:

ENST00000654629

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,090,355 - 122,367,882 (-)	Ensembl

RefSeq Acc Id:

ENST00000655138

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,222 - 122,453,719 (-)	Ensembl

RefSeq Acc Id:

ENST00000655232

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,371 - 122,067,506 (-)	Ensembl

RefSeq Acc Id:

ENST00000655288

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,860 - 122,422,788 (-)	Ensembl

RefSeq Acc Id:

ENST00000655814

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,812 - 122,453,706 (-)	Ensembl

RefSeq Acc Id:

ENST00000656226

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,698 - 122,101,509 (-)	Ensembl

RefSeq Acc Id:

ENST00000656387

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,201,021 - 122,203,342 (-)	Ensembl

RefSeq Acc Id:

ENST00000656682

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,061,998 - 122,100,470 (-)	Ensembl

RefSeq Acc Id:

ENST00000656793

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,220 - 122,180,521 (-)	Ensembl

RefSeq Acc Id:

ENST00000656868

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,292,195 - 122,367,909 (-)	Ensembl

RefSeq Acc Id:

ENST00000657554

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,366 - 122,101,689 (-)	Ensembl

RefSeq Acc Id:

ENST00000657990

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,154,726 - 122,157,108 (-)	Ensembl

RefSeq Acc Id:

ENST00000658183

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,154,726 - 122,422,850 (-)	Ensembl

RefSeq Acc Id:

ENST00000658364

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,232 - 122,105,616 (-)	Ensembl

RefSeq Acc Id:

ENST00000658452

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,856 - 122,422,849 (-)	Ensembl

RefSeq Acc Id:

ENST00000659296

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,062,395 - 122,101,581 (-)	Ensembl

RefSeq Acc Id:

ENST00000659378

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,858 - 122,309,424 (-)	Ensembl

RefSeq Acc Id:

ENST00000660148

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,351 - 122,100,482 (-)	Ensembl

RefSeq Acc Id:

ENST00000660311

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,309,337 (-)	Ensembl

RefSeq Acc Id:

ENST00000660329

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,174,358 - 122,309,507 (-)	Ensembl

RefSeq Acc Id:

ENST00000660603

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,237 - 122,157,108 (-)	Ensembl

RefSeq Acc Id:

ENST00000661432

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,331 - 122,101,733 (-)	Ensembl

RefSeq Acc Id:

ENST00000661695

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,202,880 - 122,309,434 (-)	Ensembl

RefSeq Acc Id:

ENST00000661848

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,222 - 122,367,988 (-)	Ensembl

RefSeq Acc Id:

ENST00000662950

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,144 - 122,309,451 (-)	Ensembl

RefSeq Acc Id:

ENST00000663296

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,221 - 122,156,342 (-)	Ensembl

RefSeq Acc Id:

ENST00000663802

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,861 - 122,367,905 (-)	Ensembl

RefSeq Acc Id:

ENST00000664908

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,146 - 122,203,110 (-)	Ensembl

RefSeq Acc Id:

ENST00000665051

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,861 - 122,367,974 (-)	Ensembl

RefSeq Acc Id:

ENST00000665305

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,154,793 - 122,203,003 (-)	Ensembl

RefSeq Acc Id:

ENST00000665519

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,333 - 122,102,121 (-)	Ensembl

RefSeq Acc Id:

ENST00000665673

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,126 - 122,102,203 (-)	Ensembl

RefSeq Acc Id:

ENST00000666085

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,091,117 - 122,180,632 (-)	Ensembl

RefSeq Acc Id:

ENST00000666347

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,861 - 122,309,478 (-)	Ensembl

RefSeq Acc Id:

ENST00000666485

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,395 - 122,037,057 (-)	Ensembl

RefSeq Acc Id:

ENST00000667484

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,100,532 (-)	Ensembl

RefSeq Acc Id:

ENST00000668776

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,353 - 122,204,363 (-)	Ensembl

RefSeq Acc Id:

ENST00000669306

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,100,448 (-)	Ensembl

RefSeq Acc Id:

ENST00000669472

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,232 - 122,367,760 (-)	Ensembl

RefSeq Acc Id:

ENST00000669993

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,421,543 - 122,422,857 (-)	Ensembl

RefSeq Acc Id:

ENST00000670198

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,389 - 122,101,832 (-)	Ensembl

RefSeq Acc Id:

ENST00000670374

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,366,811 - 122,367,974 (-)	Ensembl

RefSeq Acc Id:

ENST00000670396

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,089,196 - 122,453,689 (-)	Ensembl

RefSeq Acc Id:

ENST00000670520

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,859 - 122,422,860 (-)	Ensembl

RefSeq Acc Id:

ENST00000670843

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,232,854 - 122,367,974 (-)	Ensembl

RefSeq Acc Id:

ENST00000670951

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,154,755 - 122,421,831 (-)	Ensembl

RefSeq Acc Id:

ENST00000686059

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,309,474 (-)	Ensembl

RefSeq Acc Id:

ENST00000686772

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,174,358 - 122,309,460 (-)	Ensembl

RefSeq Acc Id:

ENST00000688615

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,329 - 122,101,686 (-)	Ensembl

RefSeq Acc Id:

ENST00000689894

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,100,793 (-)	Ensembl

RefSeq Acc Id:

ENST00000690059

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,105,544 (-)	Ensembl

RefSeq Acc Id:

ENST00000690151

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,100,539 (-)	Ensembl

RefSeq Acc Id:

ENST00000690198

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,101,686 (-)	Ensembl

RefSeq Acc Id:

ENST00000690515

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,308,014 - 122,309,478 (-)	Ensembl

RefSeq Acc Id:

ENST00000691884

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,100,482 (-)	Ensembl

RefSeq Acc Id:

ENST00000692224

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,308,014 - 122,309,478 (-)	Ensembl

RefSeq Acc Id:

ENST00000692610

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,101,686 (-)	Ensembl

RefSeq Acc Id:

ENST00000693154

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,100,448 (-)	Ensembl

RefSeq Acc Id:

ENST00000701811

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,201,036 - 122,309,484 (-)	Ensembl

RefSeq Acc Id:

ENST00000701835

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,101,514 - 122,102,203 (-)	Ensembl

RefSeq Acc Id:

ENST00000702205

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,201,035 - 122,207,654 (-)	Ensembl

RefSeq Acc Id:

ENST00000702309

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,331 - 122,105,353 (-)	Ensembl

RefSeq Acc Id:

ENST00000702516

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,174,366 - 122,203,063 (-)	Ensembl

RefSeq Acc Id:

ENST00000702652

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,325 - 122,101,718 (-)	Ensembl

RefSeq Acc Id:

ENST00000702800

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	122,028,328 - 122,100,448 (-)	Ensembl

RefSeq Acc Id:

NR_024430

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,203,109 (-)	NCBI
GRCh37	11	121,959,811 - 122,293,579 (-)	NCBI
Celera	11	119,120,491 - 119,234,460 (-)	RGD
HuRef	11	117,906,349 - 118,020,269 (-)	ENTREZGENE
CHM1_1	11	121,847,113 - 121,961,069 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,232,091 (-)	NCBI

Sequence:

show sequence

GGGGAGCCGCCGGAGGGCAGCTGGGGCTGCGGAATTTTGGAAGCGCAGAAGTTTTCTCCTCCTG
TCCTGTAACTGGTTTTCACTCACTCAACTGAGAGATTTCTTTGTTGCAATGATGGGGTCTAAGA
TAACACTTCTGGAGGCTGCAGGCGAGAAACACAGCTGATATCATCTTTTATTGTGTGTTGTTAT
TTGCCTAGCATTATAAATTAAGGAGGAATAGTAACAAAGAGCTTGAAGACATGCACAGCTCACA
GGCCCCGGGTGGAGGCTGGCGACATCAGACAGACAGAACCAAGACATCTGAGGGGCAACCAGGA
GGTGCGTGTGGCTGCAGAGCACACAGACTTGTCTTTGGACAAAATTGAGAAGAACTCATAAACT
TGGCTTCCTCGCTTCTGCTCCTCAGACGCGCGTGGATGATTTGAAGATATTAGCCTAACAAGAT
GGAAGCAGGTTTAAAATTTTACATAAGAAGTTACCTTTTTCAGTTGTGTTGATGTTCCTTTCAG
CTGGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACT
GCTATATTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGAC
ACCTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAG
AGACAATCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTTTCATGAGCCAAGAAC
TTTCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTTTTCCT
AGTATGGATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTAATATT
TTAAGAAACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGATCTTGA
GAGTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAA
TAATCATAGTACCACATTGGTCCACTTGACACTAACCAATCGATCATTTTTTTTTAATCAAGAA
AGCTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTAT
AGAAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCA
AGCAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAA
AGTTATAAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAA
GGAAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACACATCTT
GTTGACTTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAGTCACC
TCCTGTCTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGT
AAGGGTGATTGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTAATAATAATTGGTATT
TATTGAGTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAAT
AGGTATTATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCA
TATACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAAT
ATTGTAGTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGCAAACA
ATTAGCTATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAG
TGATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATT
TCAGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGT
AAAATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTT
TAATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGA
GTGTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGT
CTGCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTA
ACCAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAAT
GTAAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAA
TGTCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCAC
CTACATAAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAG
TGCTTCTGCACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAG
TCATTTCCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATACTTCAGCCACAGAAA
GCTAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAA
TGATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCA
GCTAAGCTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATCTGATATTTGACAATG
GTAAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCT
GTTTTAAGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAA
ACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTAT
GTGACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137175

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,102,229 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,131,229 (-)	NCBI

Sequence:

show sequence

ATTAGTAGTCAGGGAGATGCCTTAGTGCATCCAGCACTGCAAGTCAGGGATGAGACACACTACA
ACAGGAGAGGGAGCAAGCGCGAGAGGATATTAGAAGAGAGGCTTGTCTCCAAGATATGGAAGGA
AGTGAGAAATGACAGGGCTGCAAGCTTTGTATGTAGGAGCCCGGCAGGGCGGGGGAGCGGCGAG
GAGAGCCAAGTGGATTCTCAGAAAAGGGGGGAAGCCATCGAAGAGCTAAAGGTGATTAGAGGGG
GATATTGATTTCTTATTCTGCCAGAGATTTAAGCAGGCATGCGAGGAATCTGCACCATGGTTGG
CAAAAAGAGACCCGTTGCCTCCTGTAACCAGACACTCAGGCTTTCCAGGAGCCCAGGGAGCAAG
CCGAGAAGAAAGGGGGCAGTGTGGTCTAGGAAAATTCAACTTGTCGCTGATTTGTGCCTGATGC
CTGCTGTCCGTCAGCAGCCTCCCTTACAATCTTTTTTTCTCTCTCTCCTTTTTTTTTCCTTGCC
TTCTCCTTCTTCACTGAAGCCTAGGGGAGCCAGTAAAGATTAAATGTGCTTCTCAAAGGCAGCC
ACTTCATGCTGCTATGTCGAAAGGGCCATTATTATTATTATATTTTAATGGTAAAAGAGAAAAG
GAGAGAGGTTGAGCGAGCGAGAGAGAAGCTAGGTGTGATGATGACAGACTAGCTTTTCTGAGAG
GAAAAGGAAAAGGGAAGGGAGAGAAAAAGGAGAGCCTCTGAGCTCAACGGAGGATTGTGCCTGA
GAAGAACCCACAGAGCTGGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACA
AAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAG
TGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAG
AACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTT
TCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGAC
ATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCAC
AAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACAT
AGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCT
ATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTGACACTAACCAATCGATCATTT
TTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTA
GTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGA
TCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGAC
TTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGAT
TTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAAT
GAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAA
GACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCT
TCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTA
ATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCA
ACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAA
CTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATA
GTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGATATT
TTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATT
AAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATG
AAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTT
CACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTG
TTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGA
AGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGT
AGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAG
TCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTG
GTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCC
CAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTC
AAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACA
GTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTT
TTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATA
CTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTG
GCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCT
TTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATC
TGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCAT
GGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAG
TGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACT
TTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCA
ACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137176

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,100,846 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,129,846 (-)	NCBI

Sequence:

show sequence

CCCACTTCGTGTCTACCAAATGACAGCCTGGTGCTCGCTCTTGGTGATTTGGCCTTGACTTCAG
CCAAGCAGCTGATGCAGACGAAGCCTCCGTTTGCAGGACTGGCAAAGTGCACGCTAAAGAAAGA
AGGAAGAAATTTTTCAAAAAGCAGCTCTGGGGAGGTTTCATACTCCCCCCCCCCCCCCGCCTTT
TTTTAATTTTTAAGTGAATATTTTCCAAATTTGATCAGTTCCAGCCCCTCCCTCCACTCCCACC
CAACTGCCCTTTTTTCTCTCGTCAAAGCATAAGCTACAGAGTTACAGTCTCGAGATTTGGTGTA
TCGCTTCCTGCCCCCGCCTCCCCTCCCCGCCCCCGTTCTCCGTCCTCTATTGAAACACCTCGCC
CAGCCTAGCGCACTGAGAGCTCTCATTTTCCCCCCTTGCTCGGGATGGTGCCACAGGAGGCTGT
GCGGGCCCCGCTCCGCTTCGAATGGTTGTGTTGATGTTCCTTTCAGCTGGTCCTATAGTACCCC
TCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACTCT
CAAGCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAA
CACCCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAA
ACAGAAAAACTCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGT
ATTCCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTATT
AATGCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGAAT
CCTACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAATAA
AAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACATT
GGTCCACTTGACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGAT
AAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGAT
AAGTAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAG
GGGAGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAA
TATGAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGT
TCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAGAC
ATTCAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAG
GTATTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAA
TATGGAGAACTATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAAGC
ATTTTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCCAT
TTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACATTC
AGTATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACA
ATTATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTTAA
TAATCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTTCA
TGATAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTT
TTTTTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGA
GAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATC
TAAAGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGA
TGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAA
GTATGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCC
TAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAA
TGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTG
TATGATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTCTA
ACAAGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTT
TATACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAATC
CTCATGTATCCATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATC
TCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGCCA
GCTGAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTT
ATGGACAAACATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAGCT
AGCTAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATT
GTTGGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTT
TTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATGTT
CCTAACCCCCAATAAAAGCAATGTTGCATCAACTGTGAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NR_137177

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,100,846 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,129,846 (-)	NCBI

Sequence:

show sequence

CCCACTTCGTGTCTACCAAATGACAGCCTGGTGCTCGCTCTTGGTGATTTGGCCTTGACTTCAG
CCAAGCAGCTGATGCAGACGAAGCCTCCGTTTGCAGGACTGGCAAAGTGCACGCTAAAGAAAGA
AGGAAGAAATTTTTCAAAAAGCAGCTCTGGGGAGGTTTCATACTCCCCCCCCCCCCCCGCCTTT
TTTTAATTTTTAAGTGAATATTTTCCAAATTTGATCAGTTCCAGCCCCTCCCTCCACTCCCACC
CAACTGCCCTTTTTTCTCTCGTCAAAGCATAAGCTACAGAGTTACAGTCTCGAGATTTGGTGTA
TCGCTTCCTGCCCCCGCCTCCCCTCCCCGCCCCCGTTCTCCGTCCTCTATTGAAACACCTCGCC
CAGCCTAGCGCACTGAGAGCTCTCATTTTCCCCCCTTGCTCGGGATGGTGCCACAGGAGGCTGT
GCGGGCCCCGCTCCGCTTCGAATGGCTGGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAG
TGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACTATGAAGTTGAA
ACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTT
CTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAACTCAATAATGAC
ATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAA
TTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTGTTTCAAAATCC
CAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGAGAATGATTTTT
AGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTA
GTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTGACACTAACCAA
TCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAG
TTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTA
GAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGG
CAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGAACCTTGAGTGA
TGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGG
AGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGCTCTCTATACAT
ATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTAGAATTATTATC
ATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAACTATGATTTTTC
CATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATATTAACTCACTT
AAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCAAGAAAACTGAG
GTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTC
ATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCCCTTTTTATATT
CCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTAAAACTTTTCAG
TCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAA
ATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGA
TGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTT
AAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGT
GACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTT
CACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGA
GTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTG
CACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAAT
GGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATT
AAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCTTCTTAACCAAC
TTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGACTGTTTCCATAG
TACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATCCATGTAACTGA
CTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCC
TTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAG
ACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAACATCTAAATGTG
TGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCA
ATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACATCTCACATAGT
TCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACA
AAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAA
TGTTGCATCAACTGTGAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NR_137178

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,028,329 - 122,100,846 (-)	NCBI
T2T-CHM13v2.0	11	122,057,374 - 122,129,846 (-)	NCBI

Sequence:

show sequence

CCCACTTCGTGTCTACCAAATGACAGCCTGGTGCTCGCTCTTGGTGATTTGGCCTTGACTTCAG
CCAAGCAGCTGATGCAGACGAAGCCTCCGTTTGCAGGACTGGCAAAGTGCACGCTAAAGAAAGA
AGGAAGAAATTTTTCAAAAAGCAGCTCTGGGGAGGTTTCATACTCCCCCCCCCCCCCCGCCTTT
TTTTAATTTTTAAGTGAATATTTTCCAAATTTGATCAGTTCCAGCCCCTCCCTCCACTCCCACC
CAACTGCCCTTTTTTCTCTCGTCAAAGCATAAGCTACAGAGTTACAGTCTCGAGATTTGGTGTA
TCGCTTCCTGCCCCCGCCTCCCCTCCCCGCCCCCGTTCTCCGTCCTCTATTGAAACACCTCGCC
CAGCCTAGCGCACTGAGAGCTCTCATTTTCCCCCCTTGCTCGGGATGGTGCCACAGGAGGCTGT
GCGGGCCCCGCTCCGCTTCGAATGGATACAGTTAAGCTAATGATCTCGAGAGGATATCGTCCTG
GATAAGGGTGGAGCCTACGCCCAAAAACAAGATTACCTGAAAGAGAAAAGAAAGGGGGAAAACA
CACAGAGATACAGTCGGGGAGGCCACATGAAGATGGAGGCAGAGACAGGAGTGATGAGCCTGCA
AGCCAAGGAATGCCAAGGGCTGCCAGCAGCCATGAGAAGCTGAGAGACACAGAGAACGAGTCCT
CTGCCAGAGCCTCCAGAAGGAACTAACCCTGTCAATACCTTGATTTCGGACTTCTGGACTCCAG
AACTATAACCCTCCTTCCTCCACCTCACAAAAACTCACAAGCTGCAACCCTTCTGATGTCCACT
CCCACACAAACCAGCTTCAGGCCTTTTTCAAGTGGATGCTGTGGGGCACCACCTCCTTGAGGAC
CAAGGCACTCCAGCTGCCAGGAATTTGGCTGCTAACCTCACACAGCTGAGCCTTCCATGAAAAT
TGCTCTCTGCCAAAGAGAACTTCCTAGTCCAAGGTCATGTCTACTCTCCAGAGATGTGACTGGA
GTGATTTGCACCCGGATGCCTAGACTCGCCATCTGCTCAAAGACTGCTCAGAAAGCCCTCCCAT
GCATTCCCCTGCTGCATACCAGCCCACTCTGCCTGCAGCTGCTGTCTGCAGGACTTCATATCTA
TGCCACACTGTGTAAAAGCTGTGCTTCAAGAAATCACAAAAACATTTTCCTGCACCTACTACAC
AGCCTGAGTGCGGCATAAGTTGACCTTGCTTGCTAAGAAATGGGGCAAGAAATGCTTTTTTGTG
TGTGTCATGTCTGTTTGTTTTTCAATTAAGAGAGGAAAGCATTAGGCAGATGGAATGTACATGT
GAGGATGAGGAGACAGAAAACAAGTAGCCCTTTCCATCAAGATAGAGGGTTTTCTGGGGTTGCT
GGCTATTGAATGTCACTCCTGATTTCTCTTTCCAAGGCACTGTACCACCAGCCTACTGAGATTG
TGTGGGAGCTTTCATGGGGGTTGTATTTCACTGATGAAAATAAATTTTTTGCATAATGAAAAAA
AAAAAAAAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NR_137179

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,422,871 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,452,245 (-)	NCBI

Sequence:

show sequence

CTTGATGTTTTAATCCTGCCAGGAGTTTCCGTGAGGTTTTTTCAGTGGGATTATTTGTGTCCCT
GTGGCTCTTCAGGGAGCTTGCAGAATTCTAGCTAAAGATAAGAAGGGCATCGCTTCAAATGGGA
GGCCAATCAATGCAGCATTAGGAAGGCTTCATTCAGCTCAGCACCACCTTGGTGAAGATCCCGG
TGTTACACATCCAATCGTTCACCTCCTTCCAAGACTATGACATTCCAGGAAACCTTCACTGCTA
AGAGGAACTAAGATCTAGAGTATCTCCTCGAGGAAGTACAACTGACTTGTCTTTGGACAAAATT
GAGAAGAACTCATAAACTTGGCTTCCTCGCTTCTGCTCCTCAGACGCGCGTGGATGATTTGAAG
ATATTAGCCTAACAAGATGGAAGCAGGTTTAAAATTTTACATAAGAAGTTACCTTTTTCAGTTG
TGTTGATGTTCCTTTCAGCTGGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGG
ACAAAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGA
AAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCAC
TAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGA
TTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGT
GACATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTG
CACAAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACA
CATAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAG
GCTATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTGACACTAACCAATCGATCA
TTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAAT
CTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATA
AGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACT
GACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAA
GATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGA
AATGAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGA
AAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTC
CCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAACTATGATTTTTCCATTAAC
CTAATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTT
TCAACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAG
TAACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCT
ATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGAT
ATTTTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTG
ATTAAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGA
ATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATT
GTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCAC
TTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTAC
AGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATC
AGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAA
CAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCT
TTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCAT
CCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTAT
TTCAAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGC
ACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGACTGTTTCCATAGTACTTAT
GTTTTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAA
ATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCAT
GTGGCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAAT
TCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGT
ATCTGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCT
CATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATT
GAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTG
ACTTTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCA
TCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137180

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,309,487 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,338,551 (-)	NCBI

Sequence:

show sequence

GTTGCCTTTGAATGGGACCCTTGATACAAGGCTTTCATAGACCAGCCGGTGCTGATGGGGTCCG
GGACTTGACGATGGCGCCTGCTCGTTCCTGTTGTGTTCTATCTGAGGCATGATTTTCTTTCGTT
TTTGGGAGGTAGAGAGCACGGGGCAGAGGTTGCACCTGACACATTAGAACTCCGTTGTCACTGC
TGTGGCTGTTATTCCCCTCGGCAAGAGCCAAGGAGCAAACAGGACGTGAAGATCCCGGTGTTAC
ACATCCAATCGTTCACCTCCTTCCAAGACTATGACATTCCAGGAAACCTTCACTGCTAAGAGGA
ACTAAGATCTAGAGTATCTCCTCGAGGAAGTACAACTGACTTGTCTTTGGACAAAATTGAGAAG
AACTCATAAACTTGGCTTCCTCGCTTCTGCTCCTCAGACGCGCGTGGATGATTTGAAGATATTA
GCCTAACAAGATGGAAGCAGGTTTAAAATTTTACATAAGAAGTTACCTTTTTCAGTTGTGTTGA
TGTTCCTTTCAGCTGGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAG
ACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGA
TCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAGAAC
TCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTTTCA
TGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGACATT
CATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCACAAA
TGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACATAGG
GTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATT
CAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTGACACTAACCAATCGATCATTTTTT
TTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTT
AGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCA
AAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTA
CTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGATTTA
GATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAA
TACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAAGAC
TGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCTTCC
TTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTAATA
ATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCAACA
GCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTT
GCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTG
CCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGATATTTTT
CCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATTAAA
ATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATGAAG
TTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCAC
TTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTG
CAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGA
TCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGC
TTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAGTCT
ATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTT
TCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAG
AAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTCAAA
TTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACAGTG
TATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTTTTT
AAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATACTT
CAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCT
GGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCTTTC
TCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATCTGA
TATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGC
TCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAGTGA
GTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTG
TTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCAACT
GTGAA

hide sequence

RefSeq Acc Id:

NR_137181

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,203,109 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,232,091 (-)	NCBI

Sequence:

show sequence

GGGGAGCCGCCGGAGGGCAGCTGGGGCTGCGGAATTTTGGAAGCGCAGAAGTTTTCTCCTCCTG
TCCTGTAACTGGTTTTCACTCACTCAACTGAGAGATTTCTTTGTTGCAATGATGGGGTCTAAGA
TAACACTTCTGGAGGCTGCAGGCGAGAAACACAGCTGATATCATCTTTTATTGTGTGTTGTTAT
TTGCCTAGCATTATAAATTAAGGAGGAATAGTAACAAAGAGCTTGAAGACATGCACAGCTCACA
GGCCCCGGGTGGAGGCTGGCGACATCAGACAGACAGAACCAAGACATCTGAGGGGCAACCAGGA
GGTGCGTGTGGCTGCAGAGCACACAGACTTGTCTTTGGACAAAATTGAGAAGAACTCATAAACT
TGGCTTCCTCGCTTCTGCTCCTCAGCTGGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAG
TGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACTATGAAGTTGAA
ACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTT
CTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAACTCAATAATGAC
ATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAA
TTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTGTTTCAAAATCC
CAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGAGAATGATTTTT
AGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTA
GTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTGACACTAACCAA
TCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAG
TTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTA
GAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGG
CAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGAACCTTGAGTGA
TGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGG
AGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGCTCTCTATACAT
ATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTAGAATTATTATC
ATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAACTATGATTTTTC
CATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATATTAACTCACTT
AAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCAAGAAAACTGAG
GTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTC
ATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCCCTTTTTATATT
CCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTAAAACTTTTCAG
TCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAA
ATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGA
TGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTT
AAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGT
GACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTT
CACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGA
GTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTG
CACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAAT
GGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATT
AAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCTTCTTAACCAAC
TTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGACTGTTTCCATAG
TACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATCCATGTAACTGA
CTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCC
TTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAG
ACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAACATCTAAATGTG
TGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCA
ATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACATCTCACATAGT
TCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACA
AAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAA
TGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137182

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,203,109 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,232,091 (-)	NCBI

Sequence:

show sequence

GGGGAGCCGCCGGAGGGCAGCTGGGGCTGCGGAATTTTGGAAGCGCAGAAGTTTTCTCCTCCTG
TCCTGTAACTGGTTTTCACTCACTCAACTGAGAGATTTCTTTGTTGCAATGATGGGGTCTAAGA
TAACACTTCTGGAGGCTGCAGGCGAGAAACACAGCTGATATCATCTTTTATTGTGTGTTGTTAT
TTGCCTAGCATTATAAATTAAGGAGGAATAGTAACAAAGAGCTTGAAGACATGCACAGCTCACA
GGCCCCGGGTGGAGGCTGGCGACATCAGACAGACAGAACCAAGACATCTGAGGGGCAACCAGGA
GGTGCGTGTGGCTGCAGAGCACACAGACTTGTCTTTGGACAAAATTGAGAAGAACTCATAAACT
TGGCTTCCTCGCTTCTGCTCCTCAGACGCGCGTGGATGATTTGAAGATATTAGCCTAACAAGAT
GGAAGCAGGTTTAAAATTTTACATAAGAAGTTACCTTTTTCAGCTGGTCCTATAGTACCCCTCC
TCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACTCTCAA
GCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAACAC
CCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACA
GAAAAACTCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATT
CCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTATTAAT
GCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGAATCCT
ACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAG
TACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACATTGGT
CCACTTGACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAA
ATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAG
TAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGG
AGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATAT
GAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCT
TTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAGACATT
CAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTA
TTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATAT
GGAGAACTATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAAGCATT
TTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCCATTTT
ACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGT
ATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATT
ATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTTAATAA
TCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTTCATGA
TAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTT
TTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAA
TAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAA
AGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGG
AAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTA
TGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAG
TAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGA
AGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTAT
GATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTCTAACA
AGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTAT
ACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAATCCTC
ATGTATCCATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCA
TTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGCCAGCT
GAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATG
GACAAACATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAGCTAGC
TAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTT
GGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTT
AAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATGTTCCT
AACCCCCAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137183

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,180,632 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,209,605 (-)	NCBI

Sequence:

show sequence

ACAGTTTAACATTTTCTTTAGTGGTGCAACCTTGTTCTGAGATTACAGGGAATGCTGAGTTTTA
TTAGGGTTCTTTCAACAAACTCATTTAATTGTTGCTGCCCCTTAGCTAGTGCTGAGTCACTCTC
AAACTTCACAGCATTCCACGACAGCTCATCCTTCTTGACTTTCCTTTTTTTTTCCCTTTTCCTT
TTTCCTTTTTTAAGTTCTCTTAATATTTTTTATTCCCAACAGACTTGTCTTTGGACAAAATTGA
GAAGAACTCATAAACTTGGCTTCCTCGCTTCTGCTCCTCAGACGCGCGTGGATGATTTGAAGAT
ATTAGCCTAACAAGATGGAAGCAGGTTTAAAATTTTACATAAGAAGTTACCTTTTTCAGTTGTG
TTGATGTTCCTTTCAGCTGGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGAC
AAAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAA
GTGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTA
GAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATT
TTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGA
CATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCA
CAAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACA
TAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGC
TATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTGACACTAACCAATCGATCATT
TTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCT
AGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAG
ATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGA
CTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGA
TTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAA
TGAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAA
AGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTCCC
TTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAACTATGATTTTTCCATTAACCT
AATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTC
AACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTA
ACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTAT
AGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGATAT
TTTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGAT
TAAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAAT
GAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGT
TCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTT
GTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAG
AAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAG
TAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACA
GTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTT
GGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCC
CCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTT
CAAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCAC
AGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGACTGTTTCCATAGTACTTATGT
TTTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAAAT
ACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGT
GGCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTC
TTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTAT
CTGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCA
TGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGA
GTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGAC
TTTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATC
AACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137184

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,180,632 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,209,605 (-)	NCBI

Sequence:

show sequence

ACAGTTTAACATTTTCTTTAGTGGTGCAACCTTGTTCTGAGATTACAGGGAATGCTGAGTTTTA
TTAGGGTTCTTTCAACAAACTCATTTAATTGTTGCTGCCCCTTAGCTAGTGCTGAGTCACTCTC
AAACTTCACAGCATTCCACGACAGCTCATCCTTCTTGACTTTCCTTTTTTTTTCCCTTTTCCTT
TTTCCTTTTTTAAGTTCTCTTAATATTTTTTATTCCCAACAGACTTGTCTTTGGACAAAATTGA
GAAGAACTCATAAACTTGGCTTCCTCGCTTCTGCTCCTCAGTTGTGTTGATGTTCCTTTCAGCT
GGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGC
TATATTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACAC
CTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAG
ACAATCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTTTCATGAGCCAAGAACTT
TCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAG
TATGGATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTT
AAGAAACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGA
GTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATA
ATCATAGTACCACATTGGTCCACTTGACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAG
CTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAG
AAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAG
CAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAG
TTATAAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGG
AAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACACATCTTGT
TGACTTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAGTCACCTC
CTGTCTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAA
GGGTGATTGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTAATAATAATTGGTATTTA
TTGAGTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAG
GTATTATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATA
TACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATAT
TGTAGTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGCAAACAAT
TAGCTATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTG
ATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTC
AGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAA
AATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTA
ATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGT
GTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCT
GCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAAC
CAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGT
AAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATG
TCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCT
ACATAAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTG
CTTCTGCACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTC
ATTTCCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGC
TAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATG
ATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGC
TAAGCTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGT
AAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGT
TTTAAGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAAC
AGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGT
GACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137185

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,180,632 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,209,605 (-)	NCBI

Sequence:

show sequence

ACAGTTTAACATTTTCTTTAGTGGTGCAACCTTGTTCTGAGATTACAGGGAATGCTGAGTTTTA
TTAGGGTTCTTTCAACAAACTCATTTAATTGTTGCTGCCCCTTAGCTAGTGCTGAGTCACTCTC
AAACTTCACAGCATTCCACGACAGCTCATCCTTCTTGACTTTCCTTTTTTTTTCCCTTTTCCTT
TTTCCTTTTTTAAGTTCTCTTAATATTTTTTATTCCCAACAGACTTGTCTTTGGACAAAATTGA
GAAGAACTCATAAACTTGGCTTCCTCGCTTCTGCTCCTCAGACGCGCGTGGATGATTTGAAGAT
ATTAGCCTAACAAGATGGAAGCAGGTTTAAAATTTTACATAAGAAGTTACCTTTTTCAGCTGGT
CCTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTAT
ATTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTC
CTCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACA
ATCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCC
CTTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTAT
GGATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAG
AAACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTG
ACCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATC
ATAGTACCACATTGGTCCACTTGACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTA
GATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAA
TGTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAA
AAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTA
TAAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAG
GAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGA
CTTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTG
TCTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGG
TGATTGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTG
AGTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTA
TTATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATAC
AGGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGT
AGTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAG
CTATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATA
GAATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGA
CTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAAT
CCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATA
GAGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTG
GCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCC
CTTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAG
GGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAA
AAATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCC
AAAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACA
TAAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTT
CTGCACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATT
TCCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAA
AACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATT
AATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAA
GCTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAA
TTTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTT
AAGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGG
GTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGAC
TTTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137186

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,157,113 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,186,098 (-)	NCBI

Sequence:

show sequence

GAATTACTCTTGGAGTAGCAATTGCTGGATGTGCCTCTTTTGTTGAGGTGATTGGATCTTTTGG
CAAAAACCAGTGACTGCAAAGGATGAGAGAAACGATCAGAAAAACTGAAAAGCTGTAGGAGACC
AAACACTAGTGTCTCCCCTGCTTCAGGGGACACCCACTGTCAGAGTGAACGACAAAGACGCGCG
TGGATGATTTGAAGATATTAGCCTAACAAGATGGAAGCAGGTTTAAAATTTTACATAAGAAGTT
ACCTTTTTCAGTTGTGTTGATGTTCCTTTCAGCTGGTCCTATAGTACCCCTCCTCAGGAATGTC
TCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACTATGA
AGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAATTGT
GCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAACTCAA
TAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTTGT
ACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTGTTTC
AAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGAGAAT
GATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTTAAAA
TAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTGACAC
TAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTGCTTC
TAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGATAGA
GTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCATC
AAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGAACCT
TGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGTTG
TAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGCTCTC
TATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTAGAAT
TATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAACTATG
ATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATATTAA
CTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCAAGAA
AACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAGTTGC
AAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCCCTTT
TTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTAAAAC
TTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAATTGGG
AAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCAAG
ACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAAGGGG
GAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCATAAAT
TTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGCCC
TCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCAAT
TTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCTTC
TGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAAGT
TGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCTTCAA
TGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCTTCTT
AACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGACTGTT
TCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATCCATG
TAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTTTC
CATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAACAGAG
GTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAACATCT
AAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATTGTCA
GACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACATCTC
ACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCC
AAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCCAATA
AAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137187

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,157,113 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,186,098 (-)	NCBI

Sequence:

show sequence

GAATTACTCTTGGAGTAGCAATTGCTGGATGTGCCTCTTTTGTTGAGGTGATTGGATCTTTTGG
CAAAAACCAGTGACTGCAAAGGATGAGAGAAACGATCAGAAAAACTGAAAAGCTGTAGGAGACC
AAACACTAGTGTCTCCCCTGCTTCAGGGGACACCCACTGTCAGAGTGAACGACAAAGACGCGCG
TGGATGATTTGAAGATATTAGCCTAACAAGATGGAAGCAGGTTTAAAATTTTACATAAGAAGTT
ACCTTTTTCAGCTGGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGA
CTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGAT
CACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAGAACT
CTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTTTCAT
GAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGACATTC
ATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCACAAAT
GTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACATAGGG
TTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTC
AAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTGACACTAACCAATCGATCATTTTTTT
TTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTA
GAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCAA
AAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTAC
TTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGATTTAG
ATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAAT
ACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAAGACT
GCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCTTCCT
TTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTAATAA
TAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCAACAG
CCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTG
CCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTGC
CAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGATATTTTTC
CATGGCAAACAATTAGCTATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATTAAAA
TTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATGAAGT
TTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCACT
TTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGC
AATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGAT
CGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCT
TTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAGTCTA
TCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTT
CCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGA
AGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTCAAAT
TCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACAGTGT
ATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTTTTTA
AAAATATTCAGTCATTTCCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATACTTC
AGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTG
GCATTTAGTAATGATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCTTTCT
CAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATCTGAT
ATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGCT
CTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAGTGAG
TTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGT
TGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCAACTG
TGAA

hide sequence

RefSeq Acc Id:

NR_137188

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,156,371 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,185,359 (-)	NCBI

Sequence:

show sequence

CTTTTTGCAAGCAGCTGCACTGTGAGTTCGCCTTCCATTAGTAAAGGGACAATGAAGGGAAGGC
GAACCCCGCGTCCAAAACATGGCCAATGAAAGGACACTGGAATGGAAGCCAGGAATCCTGCTGT
GGTGGAGAGGCATAGACTCATGAGTCCACCACAATCGGATACTTGCTTCTTTTTAACAGCCCTA
TCAGCCGAGAGAAATAATGACTCCTGAATCATTTGACAGTAAAAAAGTTAAAATGATGTCTCAA
TGGCGCTGCATCATGCCAGACGCGCGTGGATGATTTGAAGATATTAGCCTAACAAGATGGAAGC
AGGTTTAAAATTTTACATAAGAAGTTACCTTTTTCAGCTGGTCCTATAGTACCCCTCCTCAGGA
ATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAAC
TATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAA
ATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAA
CTCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTG
TTTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTT
GTTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGG
AGAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTT
TAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTT
GACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACT
GCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAG
ATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTG
CCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATG
AACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGT
GGTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAG
CTCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTT
AGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAA
CTATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACAT
ATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGC
AAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCA
GTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACC
CCTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCT
AAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAA
TTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTT
GCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAA
AGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCA
TAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCG
GGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACT
TCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATT
GCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCA
GAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTC
TTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATC
TTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGA
CTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTAT
CCATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTC
TTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAA
CAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAA
CATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCAT
TGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCAC
ATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAG
CAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCC
CAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137189

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,102,229 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,131,229 (-)	NCBI

Sequence:

show sequence

ATTAGTAGTCAGGGAGATGCCTTAGTGCATCCAGCACTGCAAGTCAGGGATGAGACACACTACA
ACAGGAGAGGGAGCAAGCGCGAGAGGATATTAGAAGAGAGGCTTGTCTCCAAGATATGGAAGGA
AGTGAGAAATGACAGGGCTGCAAGCTTTGTATGTAGGAGCCCGGCAGGGCGGGGGAGCGGCGAG
GAGAGCCAAGTGGATTCTCAGAAAAGGGGGGAAGCCATCGAAGAGCTAAAGGTGATTAGAGGGG
GATATTGATTTCTTATTCTGCCAGAGATTTAAGCAGGCATGCGAGGAATCTGCACCATGGTTGG
CAAAAAGAGACCCGTTGCCTCCTGTAACCAGACACTCAGGCTTTCCAGGAGCCCAGGGAGCAAG
CCGAGAAGAAAGGGGGCAGTGTGGTCTAGGAAAATTCAACTTGTCGCTGATTTGTGCCTGATGC
CTGCTGTCCGTCAGCAGCCTCCCTTACAATCTTTTTTTCTCTCTCTCCTTTTTTTTTCCTTGCC
TTCTCCTTCTTCACTGAAGCCTAGGGGAGCCAGTAAAGATTAAATGTGCTTCTCAAAGGCAGCC
ACTTCATGCTGCTATGTCGAAAGGGCCATTATTATTATTATATTTTAATGGTAAAAGAGAAAAG
GAGAGAGGTTGAGCGAGCGAGAGAGAAGCTAGGTGTGATGATGACAGACTAGCTTTTCTGAGAG
GAAAAGGAAAAGGGAAGGGAGAGAAAAAGGAGAGCCTCTGAGCTCAACGGAGGATTGTGCCTGA
GAAGAACCCACAGAGTTGTGTTGATGTTCCTTTCAGCTGGTCCTATAGTACCCCTCCTCAGGAA
TGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACT
ATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAA
TTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAAC
TCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGT
TTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTG
TTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGA
GAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTT
AAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTG
ACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTG
CTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGA
TAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGC
CATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGA
ACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTG
GTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGC
TCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTA
GAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAAC
TATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATA
TTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCA
AGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAG
TTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCC
CTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTA
AAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAAT
TGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTG
CAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAA
GGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCAT
AAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGG
GCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTT
CAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTG
CTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAG
AAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCT
TCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCT
TCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGAC
TGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATC
CATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCT
TTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAAC
AGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAAC
ATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATT
GTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACA
TCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGC
AGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCC
AATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137190

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,102,229 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,131,229 (-)	NCBI

Sequence:

show sequence

ATTAGTAGTCAGGGAGATGCCTTAGTGCATCCAGCACTGCAAGTCAGGGATGAGACACACTACA
ACAGGAGAGGGAGCAAGCGCGAGAGGATATTAGAAGAGAGGCTTGTCTCCAAGATATGGAAGGA
AGTGAGAAATGACAGGGCTGCAAGCTTTGTATGTAGGAGCCCGGCAGGGCGGGGGAGCGGCGAG
GAGAGCCAAGTGGATTCTCAGAAAAGGGGGGAAGCCATCGAAGAGCTAAAGGTGATTAGAGGGG
GATATTGATTTCTTATTCTGCCAGAGATTTAAGCAGGCATGCGAGGAATCTGCACCATGGTTGG
CAAAAAGAGACCCGTTGCCTCCTGTAACCAGACACTCAGGCTTTCCAGGAGCCCAGGGAGCAAG
CCGAGAAGAAAGGGGGCAGTGTGGTCTAGGAAAATTCAACTTGTCGCTGATTTGTGCCTGATGC
CTGCTGTCCGTCAGCAGCCTCCCTTACAATCTTTTTTTCTCTCTCTCCTTTTTTTTTCCTTGCC
TTCTCCTTCTTCACTGAAGCCTAGGGGAGCCAGTAAAGATTAAATGTGCTTCTCAAAGGCAGCC
ACTTCATGCTGCTATGTCGAAAGGGCCATTATTATTATTATATTTTAATGGTAAAAGAGAAAAG
GAGAGAGGTTGAGCGAGCGAGAGAGAAGCTAGGTGTGATGATGACAGACTAGCTTTTCTGAGAG
GAAAAGGAAAAGGGAAGGGAGAGAAAAAGGAGAGCCTCTGAGCTCAACGGAGGATTGTGCCTGA
GAAGAACCCACAGAGGAGGCTGTGCGGGCCCCGCTCCGCTTCGAATGGTTGTGTTGATGTTCCT
TTCAGCTGGTCCTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAG
AGACTGCTATATTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTG
AAGACACCTCCTCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGA
ACAAGAGACAATCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTTTCATGAGCCA
AGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTT
TTCCTAGTATGGATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTA
ATATTTTAAGAAACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGAT
CTTGAGAGTGACCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGG
TAAAATAATCATAGTACCACATTGGTCCACTTGACACTAACCAATCGATCATTTTTTTTTAATC
AAGAAAGCTAGATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAA
GTTATAGAAATGTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAA
AACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGG
AAGAAAGTTATAAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAAT
GGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACAC
ATCTTGTTGACTTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAG
TCACCTCCTGTCTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAG
TAAGTAAGGGTGATTGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTAATAATAATTG
GTATTTATTGAGTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGC
AAAATAGGTATTATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAG
TGCCATATACAGGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTT
GCAATATTGTAGTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGC
AAACAATTAGCTATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGC
TGGAGTGATAGAATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCA
GCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTC
TATGTAAAATCCCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCC
CTTTTTAATAGAGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACT
TTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCA
CTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGG
CAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACC
TCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATG
CATAATGTCCAAAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAG
TTCACCTACATAAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTT
GTAAGTGCTTCTGCACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATA
TTCAGTCATTTCCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATACTTCAGCCAC
AGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTT
AGTAATGATTAATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGG
AGTCAGCTAAGCTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATCTGATATTTGA
CAATGGTAAATTTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCC
GTCCTGTTTTAAGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATA
AATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACAT
TTTATGTGACTTTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137191

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,102,229 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,131,229 (-)	NCBI

Sequence:

show sequence

ATTAGTAGTCAGGGAGATGCCTTAGTGCATCCAGCACTGCAAGTCAGGGATGAGACACACTACA
ACAGGAGAGGGAGCAAGCGCGAGAGGATATTAGAAGAGAGGCTTGTCTCCAAGATATGGAAGGA
AGTGAGAAATGACAGGGCTGCAAGCTTTGTATGTAGGAGCCCGGCAGGGCGGGGGAGCGGCGAG
GAGAGCCAAGTGGATTCTCAGAAAAGGGGGGAAGCCATCGAAGAGCTAAAGGTGATTAGAGGGG
GATATTGATTTCTTATTCTGCCAGAGATTTAAGCAGGCATGCGAGGAATCTGCACCATGGTTGG
CAAAAAGAGACCCGTTGCCTCCTGTAACCAGACACTCAGGCTTTCCAGGAGCCCAGGGAGCAAG
CCGAGAAGAAAGGGGGCAGTGTGGTCTAGGAAAATTCAACTTGTCGCTGATTTGTGCCTGATGC
CTGCTGTCCGTCAGCAGCCTCCCTTACAATCTTTTTTTCTCTCTCTCCTTTTTTTTTCCTTGCC
TTCTCCTTCTTCACTGAAGCCTAGGGGAGCCAGTAAAGATTAAATGTGCTTCTCAAAGGCAGCC
ACTTCATGCTGCTATGTCGAAAGGGCCATTATTATTATTATATTTTAATGGTAAAAGAGAAAAG
GAGAGAGGTTGAGCGAGCGAGAGAGAAGCTAGGTGTGATGATGACAGACTAGCTTTTCTGAGAG
GAAAAGGAAAAGGGAAGGGAGAGAAAAAGGAGAGCCTCTGAGCTCAACGGAGGATTGTGCCTGA
GAAGAACCCACAGAGGAGGCTGTGCGGGCCCCGCTCCGCTTCGAATGGCTGGTCCTATAGTACC
CCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACT
CTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGA
AACACCCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAG
AAACAGAAAAACTCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGT
GTATTCCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTA
TTAATGCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGA
ATCCTACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAAT
AAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACA
TTGGTCCACTTGACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAG
ATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAG
ATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTC
AGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAA
AATATGAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGA
GTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAG
ACATTCAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCC
AGGTATTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGAC
AATATGGAGAACTATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAA
GCATTTTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCC
ATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACAT
TCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCA
CAATTATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTT
AATAATCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTT
CATGATAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTT
TTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTT
GAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAA
TCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGG
GATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATT
AAGTATGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTG
CCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGC
AATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATG
TGTATGATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTC
TAACAAGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATG
TTTATACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAA
TCCTCATGTATCCATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAA
TCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGC
CAGCTGAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTAC
TTATGGACAAACATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAG
CTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAA
TTGTTGGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTT
TTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATG
TTCCTAACCCCCAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137192

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,367,988 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,397,033 (-)	NCBI

Sequence:

show sequence

AGTGCGGGGCTAAGCATGCTCAGTGTAAATTCTCCTGGAGCCTGTCAAGCTATGTTTGAACTCG
TTCCAGGATAGTGGATTTACTTTTTTTTCCCCACCAGGAAGAATACTCGATTAGACTGCATTTT
GCCTTGCTTTTCCTTCTCCCTTTCTCTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTT
TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTTTCTTTCTCTCTCTCTCTCTCTTTCTT
TCTTTCCTTTCTTTTCTTTCTTTCCTCTTTCTCTTTCCTTCTTTCTTTTTTTCTTCTTTCTTTC
CTTCCTTCCTTCCATCTTTCTTTTCTTTCTTTCCATTTTTTTTTTCCTCCAGAAGAATGGAAAC
AGTATTCTTTTCCGATCAGTTCAGTAATACAATGTCCTTCAGTGTCCATATGAGCATTTCAGTG
GAGAAGAAAAGAAACTTTGCTACCTGGGAACTGAAGACTACTTAGTGAAGATCCCGGTGTTACA
CATCCAATCGTTCACCTCCTTCCAAGACTATGACATTCCAGGAAACCTTCACTGCTAAGAGGAA
CTAAGATCTAGAGTATCTCCTCGAGGAAGTACAACTGACTTGTCTTTGGACAAAATTGAGAAGA
ACTCATAAACTTGGCTTCCTCGCTTCTGCTCCTCAGCTGGTCCTATAGTACCCCTCCTCAGGAA
TGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACT
ATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAA
TTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAAC
TCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGT
TTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTG
TTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGA
GAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTT
AAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTG
ACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTG
CTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGA
TAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGC
CATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGA
ACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTG
GTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGC
TCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTA
GAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAAC
TATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATA
TTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCA
AGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAG
TTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCC
CTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTA
AAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAAT
TGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTG
CAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAA
GGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCAT
AAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGG
GCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTT
CAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTG
CTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAG
AAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCT
TCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCT
TCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGAC
TGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATC
CATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCT
TTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAAC
AGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAAC
ATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATT
GTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACA
TCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGC
AGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCC
AATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137193

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,309,487 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,338,551 (-)	NCBI

Sequence:

show sequence

GTTGCCTTTGAATGGGACCCTTGATACAAGGCTTTCATAGACCAGCCGGTGCTGATGGGGTCCG
GGACTTGACGATGGCGCCTGCTCGTTCCTGTTGTGTTCTATCTGAGGCATGATTTTCTTTCGTT
TTTGGGAGGTAGAGAGCACGGGGCAGAGGTTGCACCTGACACATTAGAACTCCGTTGTCACTGC
TGTGGCTGTTATTCCCCTCGGCAAGAGCCAAGGAGCAAACAGGACGTGAAGATCCCGGTGTTAC
ACATCCAATCGTTCACCTCCTTCCAAGACTATGACATTCCAGGAAACCTTCACTGCTAAGAGGA
ACTAAGATCTAGAGTATCTCCTCGAGGAAGTACAACTGACTTGTCTTTGGACAAAATTGAGAAG
AACTCATAAACTTGGCTTCCTCGCTTCTGCTCCTCAGACGCGCGTGGATGATTTGAAGATATTA
GCCTAACAAGATGGAAGCAGGTTTAAAATTTTACATAAGAAGTTACCTTTTTCAGCTGGTCCTA
TAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTG
ATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCT
GCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCT
TTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTC
CTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGAT
ATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAAC
AAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCT
ACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAG
TACCACATTGGTCCACTTGACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATT
CTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTT
TGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGA
TGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAA
ACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGA
AAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTA
AACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTC
TCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGAT
TGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTT
CTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTAT
TATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGG
CTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTC
AATGTCACAATTATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTAT
TTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAAT
GTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTG
TTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCA
AATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGG
CAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAG
AGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTC
CTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAG
CTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAAT
AGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAG
TTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAA
TCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGC
ACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCT
ACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACT
GAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATA
ATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTG
GGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTC
CACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGC
ATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTT
TTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTG
TCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137194

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,156,371 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,185,359 (-)	NCBI

Sequence:

show sequence

CTTTTTGCAAGCAGCTGCACTGTGAGTTCGCCTTCCATTAGTAAAGGGACAATGAAGGGAAGGC
GAACCCCGCGTCCAAAACATGGCCAATGAAAGGACACTGGAATGGAAGCCAGGAATCCTGCTGT
GGTGGAGAGGCATAGACTCATGAGTCCACCACAATCGGATACTTGCTTCTTTTTAACAGCCCTA
TCAGCCGAGAGAAATAATGACTCCTGAATCATTTGACAGTAAAAAAGTTAAAATGATGTCTCAA
TGGCGCTGCATCATGCCAGACGCGCGTGGATGATTTGAAGATATTAGCCTAACAAGATGGAAGC
AGGTTTAAAATTTTACATAAGAAGTTACCTTTTTCAGTTGTGTTGATGTTCCTTTCAGCTGGTC
CTATAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATA
TTGATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCC
TCTGCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAA
TCTTTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCC
TTCCTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATG
GATATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGA
AACAAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGA
CCTACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCA
TAGTACCACATTGGTCCACTTGACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAG
ATTCTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAAT
GTTTGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAA
AGATGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTAT
AAAACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGG
AGAAAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGAC
TTAAACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGT
CTCTCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGT
GATTGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGA
GTTCTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTAT
TATTATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACA
GGGCTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTA
GTCAATGTCACAATTATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGC
TATTTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAG
AATGTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGAC
TTGTTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATC
CCAAATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAG
AGGCAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGG
CAGAGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCC
TTCCTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGG
GAGCTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAA
AATAGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCA
AAGTTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACAT
AAATCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTC
TGCACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTT
CCTACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAA
ACTGAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTA
ATAATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAG
CTGGGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAAT
TTCCACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTA
AGCATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGG
TTTTTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACT
TTGTCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137195

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,105,616 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,134,617 (-)	NCBI

Sequence:

show sequence

AGTGGGAGGTGGGGCCAGTCTGGCACAGTCTGTGGGTTTGAAAGGAGCTGGGCGGGTTGGAGAA
TGCCAGTCAGCCTTTGTAGTTCTGAGCTCAGAGAGGGGGTGACACATACTGGGCTTCAGGTCAG
AAGCCTGGCTTGGGTGGCTTTTGGAGAAATTTTCCCTCTGCTCCCAAACTCTTAAAAGGTGCTC
ATCACACCACTGGCCTCCAATCACAGCATAAGCACGTGTTCCAAAGGCCATCCTCCAGCAGAGA
TTTCGGCAGTGGTACCTGTTGGCTGGCTCATGGGGTCCTTTCCTTTTTCCATTCCCTGGAAGCC
GTCAACTGGACTGAATACAACATCTTTGCGTCTTTTTCTTCACCCTCCCCACATGCTTGCATCT
CCCAGACTCCTAGGGTTAATCCCCAGGACAACCTTGCTTTGAAAGAAAAAATGTGGTGAGCCTA
CTTGAAGATTTGGATTCCAAGAGGCCTCTGTCTGTCCTGCCTCAGCCAGAGCCAGACAGCCAGC
TCAAGGAGATGGGCAATTTACAGAGAAAGCAGCACTGGTCCTATAGTACCCCTCCTCAGGAATG
TCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTGATGGACTCTCAAGCCAACTAT
GAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCTGCTAAGAAACACCCCCAAATT
GTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCTTTTCAAGAAACAGAAAAACTC
AATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTCCTCATGTGTATTCCTCTGTTT
GTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGATATGCTTATTAATGCACTTGTT
TCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAACAAAATGAATCCTACAAGGAGA
ATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCTACAGAATAAAAGTACTTTTAA
AATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAGTACCACATTGGTCCACTTGAC
ACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATTCTATCAGATAAAATCACTGCT
TCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTTTGCAAAGATAAGTAACAGATA
GAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGATGAGTTCAGGGGAGTTTGCCA
TCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAAACAGGAAAATATGAGATGAAC
CTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGAAAATGGAGTTCTTTAGGTGGT
TGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTAAACCCAGACATTCAGCAGCTC
TCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTCTCACCCCAGGTATTACTTAGA
ATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGATTGGTGACAATATGGAGAACTA
TGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTTCTGTTAAGCATTTTACATATT
AACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTATTATCCCCATTTTACAGGCAAG
AAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGGCTCACATTCAGTATTGCAGTT
GCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTCAATGTCACAATTATTACCCCT
TTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTATTTCATTTAATAATCACCTAAA
ACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAATGTATTTTCATGATAGAAATTG
GGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTGTTTTTTTTTTTTTTTTTTGCA
AGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCAAATCCTTGAGAATAAAAAAGG
GGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGGCAATAAATCTAAAGGCCATAA
ATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAGAGTAAGGGATGGAAACCGGGC
CCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTCCTAAATTAAGTATGCACTTCA
ATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAGCTTTGTGCCTAGTAGATTGCT
TCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAATAGCTAGCAATGAAGTCCAGAA
GTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAGTTGTATGTGTATGATGTCTTC
AATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAATCATTTCTAACAAGCATCTTC
TTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGCACGAATGTTTATACATGACTG
TTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCTACTATAATCCTCATGTATCCA
TGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACTGAGCAAATCTCATTCTTCTTT
TCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATAATATGGCCAGCTGAATAACAG
AGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTGGGTCTACTTATGGACAAACAT
CTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTCCACTTAGCTAGCTAGCATTGT
CAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGCATGATAATTGTTGGCCACATC
TCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTTTTTTTTTTTTTTAAAGAGCAG
CCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTGTCATATGTTCCTAACCCCCAA
TAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

RefSeq Acc Id:

NR_137196

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	122,089,103 - 122,105,616 (-)	NCBI
T2T-CHM13v2.0	11	122,118,107 - 122,134,617 (-)	NCBI

Sequence:

show sequence

AGTGGGAGGTGGGGCCAGTCTGGCACAGTCTGTGGGTTTGAAAGGAGCTGGGCGGGTTGGAGAA
TGCCAGTCAGCCTTTGTAGTTCTGAGCTCAGAGAGGGGGTGACACATACTGGGCTTCAGGTCAG
AAGCCTGGCTTGGGTGGCTTTTGGAGAAATTTTCCCTCTGCTCCCAAACTCTTAAAAGGTGCTC
ATCACACCACTGGCCTCCAATCACAGCATAAGCACGTGTTCCAAAGGCCATCCTCCAGCAGAGA
TTTCGGCAGTGGTACCTGTTGGCTGGCTCATGGGGTCCTTTCCTTTTTCCATTCCCTGGAAGCC
GTCAACTGGACTGAATACAACATCTTTGCGTCTTTTTCTTCACCCTCCCCACATGCTTGCATCT
CCCAGACTCCTAGGGTTAATCCCCAGGACAACCTTGCTTTGAAAGAAAAAATGTGGTGAGCCTA
CTTGAAGATTTGGATTCCAAGAGGCCTCTGTCTGTCCTGCCTCAGCCAGAGCCAGACAGCCAGC
TCAAGGAGATGGGCAATTTACAGAGAAAGCAGCATTGTGTTGATGTTCCTTTCAGCTGGTCCTA
TAGTACCCCTCCTCAGGAATGTCTCCCCAGTGCAAGGACAAAGACTGAAGAGACTGCTATATTG
ATGGACTCTCAAGCCAACTATGAAGTTGAAACAAAGAAAGTGATCACCTGAAGACACCTCCTCT
GCTAAGAAACACCCCCAAATTGTGCAGCTTCTGCCACTAGAACTCTCAGAACAAGAGACAATCT
TTTCAAGAAACAGAAAAACTCAATAATGACATCTAGATTTTCATGAGCCAAGAACTTTCCCTTC
CTCATGTGTATTCCTCTGTTTGTACTTAAATTCATGTGACATTCATTTTTTTCCTAGTATGGAT
ATGCTTATTAATGCACTTGTTTCAAAATCCCAAATTGCACAAATGTGTTAATATTTTAAGAAAC
AAAATGAATCCTACAAGGAGAATGATTTTTAGCCACACATAGGGTTGGATCTTGAGAGTGACCT
ACAGAATAAAAGTACTTTTAAAATAAAGTAGTCAGAGGCTATTCAAAGGGTAAAATAATCATAG
TACCACATTGGTCCACTTGACACTAACCAATCGATCATTTTTTTTTAATCAAGAAAGCTAGATT
CTATCAGATAAAATCACTGCTTCTAAAGAGTTTAAATCTAGTTAGAAAAAGTTATAGAAATGTT
TGCAAAGATAAGTAACAGATAGAGTCAGTAGAGGATAAGATCAAAAACAAAACCAAGCAAAAGA
TGAGTTCAGGGGAGTTTGCCATCAAGTTGGCAAAACTGACTTACTTAGGGAAGAAAGTTATAAA
ACAGGAAAATATGAGATGAACCTTGAGTGATGTGGAAGATTTAGATAAATGGAAAGGAAGGAGA
AAATGGAGTTCTTTAGGTGGTTGTAATTGGAGGAGGAAATGAATACACACATCTTGTTGACTTA
AACCCAGACATTCAGCAGCTCTCTATACATATCTGGAAAAGACTGCACAGTCACCTCCTGTCTC
TCACCCCAGGTATTACTTAGAATTATTATCATATTTCCCTTCCTTTAAAGTAAGTAAGGGTGAT
TGGTGACAATATGGAGAACTATGATTTTTCCATTAACCTAATAATAATTGGTATTTATTGAGTT
CTGTTAAGCATTTTACATATTAACTCACTTAAGCCTTTCAACAGCCTTGCAAAATAGGTATTAT
TATCCCCATTTTACAGGCAAGAAAACTGAGGTTTAAGTAACTTGCCGAAGTGCCATATACAGGG
CTCACATTCAGTATTGCAGTTGCAAAGCTCATGATCTATAGTGCCAAGTTGCAATATTGTAGTC
AATGTCACAATTATTACCCCTTTTTATATTCCTTGATATTTTTCCATGGCAAACAATTAGCTAT
TTCATTTAATAATCACCTAAAACTTTTCAGTCTTCTGATTAAAATTACGCTGGAGTGATAGAAT
GTATTTTCATGATAGAAATTGGGAAAAAAAATGGGGAATGAAGTTTATCAGCATTTCAGACTTG
TTTTTTTTTTTTTTTTTTGCAAGACTTTGATGAGATTGTTCACTTTTGTCTATGTAAAATCCCA
AATCCTTGAGAATAAAAAAGGGGGAGGTTTAAGTCACTTGTTGCAATGCCCTTTTTAATAGAGG
CAATAAATCTAAAGGCCATAAATTTAGAGTGACTTACAGAAGATCGAACTTTGGAGTGTGGCAG
AGTAAGGGATGGAAACCGGGCCCTCCAGTTCACTATCAGTAGCTTTTGCACTGGTCTGCCCTTC
CTAAATTAAGTATGCACTTCAATTTGATGAGTGGAAACAGTCTATCTGGGCAGTAACCAGGGAG
CTTTGTGCCTAGTAGATTGCTTCTGTTCTGCACTTCTTTGGTTTCCCACCTCAATGTAAAAAAT
AGCTAGCAATGAAGTCCAGAAGTTGTCAATGGTTCATCCCCAGAAGAATGCATAATGTCCAAAG
TTGTATGTGTATGATGTCTTCAATGGTATTAAGTTATTTCAAATTCTTAGTTCACCTACATAAA
TCATTTCTAACAAGCATCTTCTTAACCAACTTTATGCACAGTGTATGTTTGTAAGTGCTTCTGC
ACGAATGTTTATACATGACTGTTTCCATAGTACTTATGTTTTTAAAAATATTCAGTCATTTCCT
ACTATAATCCTCATGTATCCATGTAACTGACTCAAAAATACTTCAGCCACAGAAAGCTAAAACT
GAGCAAATCTCATTCTTCTTTTCCATCCCCTTTGCATGTGGCTGGCATTTAGTAATGATTAATA
ATATGGCCAGCTGAATAACAGAGGTTTGAGACACAATTCTTTCTCAAAGGAGTCAGCTAAGCTG
GGTCTACTTATGGACAAACATCTAAATGTGTGGAAGTATCTGATATTTGACAATGGTAAATTTC
CACTTAGCTAGCTAGCATTGTCAGACTTCAATCTCCTCATGGCTCTGGCCGTCCTGTTTTAAGC
ATGATAATTGTTGGCCACATCTCACATAGTTCTCATTGAGTGAGTTCATAAATAAACAGGGTTT
TTTTTTTTTTTTAAAGAGCAGCCAAGCACAAAGTGTGACTTTGTTGACATTTTATGTGACTTTG
TCATATGTTCCTAACCCCCAATAAAAGCAATGTTGCATCAACTGTGAA

hide sequence

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:39522	AgrOrtholog
COSMIC	MIR100HG	COSMIC
Ensembl Genes	ENSG00000255248	Ensembl, ENTREZGENE
Ensembl Transcript	ENST00000524376	ENTREZGENE
	ENST00000529823	ENTREZGENE
	ENST00000531071	ENTREZGENE
	ENST00000532890	ENTREZGENE
	ENST00000648209	ENTREZGENE
	ENST00000650497	ENTREZGENE
	ENST00000653167	ENTREZGENE
	ENST00000654519	ENTREZGENE
	ENST00000656793	ENTREZGENE
	ENST00000658364	ENTREZGENE
	ENST00000660603	ENTREZGENE
	ENST00000661848	ENTREZGENE
	ENST00000662950	ENTREZGENE
	ENST00000663296	ENTREZGENE
	ENST00000664908	ENTREZGENE
GTEx	ENSG00000255248	GTEx
HGNC ID	HGNC:39522	ENTREZGENE
Human Proteome Map	MIR100HG	Human Proteome Map
NCBI Gene	399959	ENTREZGENE
OMIM	615965	OMIM
RNAcentral	URS0000A765BD	RNACentral
	URS0000A76617	RNACentral
	URS0000A76642	RNACentral
	URS0000A76766	RNACentral
	URS0000A7689E	RNACentral
	URS0000A768D4	RNACentral
	URS0000A76931	RNACentral
	URS0000A76A56	RNACentral
	URS0000A76B28	RNACentral
	URS0000A76BF1	RNACentral
	URS0000A76C00	RNACentral
	URS0000A76C13	RNACentral
	URS0000A76E00	RNACentral
	URS0000A76E1B	RNACentral
	URS0000A76F01	RNACentral
	URS0000A76F58	RNACentral
	URS0000A76F9C	RNACentral
	URS0000A7701D	RNACentral
	URS0000A770A1	RNACentral
	URS0000A7737F	RNACentral
	URS0000A773F0	RNACentral
	URS0000A774C6	RNACentral
	URS0000A77780	RNACentral

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2017-05-02	MIR100HG	mir-100-let-7a-2-mir-125b-1 cluster host gene		mir-100-let-7a-2 cluster host gene	Symbol and/or name change	5135510	APPROVED
2015-02-24	MIR100HG	mir-100-let-7a-2 cluster host gene		mir-100-let-7a-2 cluster host gene (non-protein coding)	Symbol and/or name change	5135510	APPROVED

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

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

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

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

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

Imported Human Phenotype Annotations - ClinVar