Variant report

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs1015505	1.00[ASW][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs16985070	0.85[ASW][hapmap]
rs16985073	0.85[ASW][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	nsv916408	chrX:103552340-104347979	Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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