Variant report

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

rs_ID	r²[population]
rs11174276	0.88[CHB][hapmap]
rs11174279	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1121705	1.00[JPT][hapmap]
rs11609846	0.84[ASN][1000 genomes]
rs1371918	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1440723	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs1440724	1.00[JPT][hapmap]
rs1561629	1.00[JPT][hapmap]
rs17125609	1.00[JPT][hapmap]
rs17125631	1.00[JPT][hapmap]
rs17704825	1.00[JPT][hapmap]
rs17705406	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs1838380	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4763004	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4763131	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs4965015	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7314952	1.00[JPT][hapmap]
rs9668407	1.00[JPT][hapmap]
rs9668420	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs9668428	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs9669020	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs9669149	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs9669794	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs9737644	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs9739051	0.86[CHB][hapmap];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	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No data

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