Variant report

Variant	rs5981589
Chromosome Location	chrX:73321892-73321893
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1151599	1.00[CHB][hapmap]
rs1151602	1.00[CHB][hapmap]
rs1341326	1.00[CHB][hapmap]
rs174164	0.82[CHB][hapmap];0.92[YRI][hapmap]
rs2066449	1.00[CHB][hapmap]
rs4892491	1.00[CHB][hapmap];0.84[MEX][hapmap]
rs5981258	1.00[CHB][hapmap]
rs5981594	1.00[CHB][hapmap];0.97[GIH][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.92[YRI][hapmap]
rs5981595	0.82[CHB][hapmap]
rs604174	1.00[CHB][hapmap];0.84[MEX][hapmap]
rs6607463	0.80[ASW][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.92[YRI][hapmap]
rs6647038	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap]
rs6647445	1.00[CHB][hapmap]
rs6647446	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[MEX][hapmap]
rs6647448	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs6647454	1.00[CHB][hapmap]
rs6655556	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3364045	chrX:72896383-73699363	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	301 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:73306800-73353000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chrX:73319000-73340800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chrX:73319200-73322400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chrX:73319400-73323400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chrX:73319600-73347800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chrX:73320400-73343000	Weak transcription	Left Ventricle	heart
7	chrX:73321000-73323200	Weak transcription	Aorta	Aorta
8	chrX:73321400-73322800	Weak transcription	Fetal Intestine Small	intestine
9	chrX:73321400-73325000	Weak transcription	Ovary	ovary
10	chrX:73321600-73349400	Weak transcription	Right Ventricle	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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