Variant report

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs3908421	0.92[CEU][hapmap];0.89[JPT][hapmap]
rs5984857	0.91[CEU][hapmap];0.88[JPT][hapmap]
rs5984873	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6615320	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][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	nsv432350	chrX:91158935-91590765	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No data

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