Variant report

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

rs_ID	r²[population]
rs10484792	1.00[YRI][hapmap]
rs10485436	0.84[AMR][1000 genomes]
rs13191240	1.00[JPT][hapmap]
rs13191563	1.00[JPT][hapmap]
rs13197569	1.00[JPT][hapmap]
rs13205016	1.00[JPT][hapmap]
rs13205140	1.00[JPT][hapmap]
rs13219339	1.00[JPT][hapmap]
rs13220538	1.00[YRI][hapmap]
rs16900400	1.00[JPT][hapmap]
rs2200088	1.00[JPT][hapmap]
rs3757045	1.00[JPT][hapmap]
rs3798980	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs3798996	1.00[JPT][hapmap]
rs3799023	1.00[JPT][hapmap]
rs3823061	1.00[JPT][hapmap]
rs6903686	1.00[JPT][hapmap]
rs6908180	1.00[JPT][hapmap]
rs6919909	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6934473	1.00[JPT][hapmap]
rs7761270	1.00[JPT][hapmap]
rs7767118	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470831	chr6:69581991-69654650	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv886136	chr6:69598297-69654650	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No data

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