Variant report

Variant	rs370713
Chromosome Location	chrX:138642393-138642394
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs440051	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532935	chrX:138281469-138764448	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv521021	chrX:138642393-138648526	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv528242	chrX:138642393-138672695	Enhancers Weak transcription Bivalent Enhancer Strong transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:138640600-138642600	Weak transcription	Liver	Liver
2	chrX:138641800-138642400	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chrX:138641800-138642600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chrX:138642000-138642400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chrX:138642000-138642400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chrX:138642000-138643000	Enhancers	HSMM	muscle

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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