Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1348163	0.99[ASN][1000 genomes]
rs1441465	0.99[ASN][1000 genomes]
rs1441468	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs34363944	0.99[ASN][1000 genomes]
rs34691836	0.99[ASN][1000 genomes]
rs35737844	0.99[ASN][1000 genomes]
rs493102	0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.99[ASN][1000 genomes]
rs499085	0.97[ASN][1000 genomes]
rs501969	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs502443	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs504651	0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs515937	0.97[ASN][1000 genomes]
rs516729	0.95[ASN][1000 genomes]
rs518446	0.95[ASN][1000 genomes]
rs522243	0.95[ASN][1000 genomes]
rs531021	0.81[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs544510	0.81[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs547663	0.81[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs566701	0.97[ASN][1000 genomes]
rs62172826	0.99[ASN][1000 genomes]

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	nsv583193	chr2:141365171-141415043	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No data

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