Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11092531	0.82[CEU][hapmap]
rs2009995	0.81[CEU][hapmap]
rs2392686	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs4826890	0.88[CEU][hapmap]
rs4826914	0.82[CEU][hapmap]
rs4826915	0.87[CEU][hapmap]
rs4826916	0.82[CEU][hapmap]
rs5916723	0.88[CEU][hapmap]
rs5916724	0.88[CEU][hapmap]
rs5916729	0.88[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap]
rs5916730	0.81[CHB][hapmap]
rs5916866	0.88[CEU][hapmap]
rs5916870	0.88[CEU][hapmap]
rs5916873	0.82[CEU][hapmap]
rs5916874	0.82[CEU][hapmap]
rs5916875	0.88[CEU][hapmap]
rs5916876	0.88[CEU][hapmap]
rs5916887	0.81[CHB][hapmap]
rs5962466	0.81[CEU][hapmap]
rs5962469	0.82[CEU][hapmap]
rs6616565	0.88[CEU][hapmap]
rs6616567	0.82[CEU][hapmap]
rs6616570	0.88[CEU][hapmap]
rs6616576	0.88[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap]
rs6621930	0.88[CEU][hapmap]
rs6621931	0.88[CEU][hapmap]
rs6621938	0.82[CEU][hapmap]
rs6621941	0.88[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap]
rs6621944	0.81[CHB][hapmap];0.80[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	nsv432352	chrX:104346855-104831855	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No data

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