Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11123020	0.93[TSI][hapmap]
rs12996212	1.00[AFR][1000 genomes]
rs13017140	1.00[AFR][1000 genomes]
rs13426564	0.88[JPT][hapmap]
rs1439140	0.95[EUR][1000 genomes]
rs17010759	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs17010772	0.82[CEU][hapmap];0.93[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17010799	0.82[CEU][hapmap];0.87[CHD][hapmap];0.91[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap]
rs17010805	0.82[CEU][hapmap]
rs17010807	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17010907	0.94[JPT][hapmap]
rs17010972	1.00[ASW][hapmap]
rs17269024	1.00[AFR][1000 genomes]
rs34711614	1.00[AFR][1000 genomes]
rs61605355	0.98[EUR][1000 genomes]
rs71428132	1.00[AFR][1000 genomes]
rs71428134	1.00[AFR][1000 genomes]
rs71428135	1.00[AFR][1000 genomes]
rs7584999	0.94[JPT][hapmap];0.95[EUR][1000 genomes]
rs951031	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs960536	1.00[ASW][hapmap]
rs960537	1.00[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	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No data

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