Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1156923	1.00[CHB][hapmap]
rs1321380	1.00[CHB][hapmap]
rs1321381	1.00[CHB][hapmap]
rs1321388	1.00[CHB][hapmap]
rs16984799	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs16984800	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs16984807	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs210726	0.82[CHB][hapmap]
rs210729	0.82[CHB][hapmap]
rs210734	0.82[CHB][hapmap]
rs2213338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs222582	1.00[CHB][hapmap]
rs222584	1.00[CHB][hapmap]
rs222585	1.00[CHB][hapmap]
rs222597	1.00[CHB][hapmap]
rs222599	1.00[CHB][hapmap]
rs222601	1.00[CHB][hapmap]
rs4826920	1.00[CHB][hapmap]
rs5916899	1.00[CHB][hapmap]
rs5916903	1.00[CHB][hapmap]
rs5916928	0.82[CHB][hapmap]
rs5962536	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs6523840	1.00[CHB][hapmap]
rs6616582	1.00[CHB][hapmap]
rs7050641	1.00[CEU][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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