Variant report

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

rs_ID	r²[population]
rs1034572	0.85[CEU][hapmap]
rs11760238	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11761138	1.00[JPT][hapmap]
rs11762662	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12333888	0.96[CEU][hapmap]
rs12533385	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs12539136	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs13232636	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs13234705	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs13238097	1.00[JPT][hapmap]
rs17137948	0.85[CEU][hapmap]
rs17335819	1.00[JPT][hapmap]
rs2073790	0.97[ASN][1000 genomes]
rs2073792	0.92[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2188172	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs6949376	0.84[CEU][hapmap];0.80[CHB][hapmap]
rs6949536	0.92[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6949602	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6949811	0.87[CEU][hapmap]
rs6955069	0.93[CEU][hapmap]
rs6965697	0.85[CEU][hapmap]
rs756669	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	nsv888925	chr7:104047599-104170560	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No data

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