Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10877781	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs11174276	0.90[CHB][hapmap]
rs11174279	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1121705	1.00[JPT][hapmap]
rs1440723	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	1.00[JPT][hapmap]
rs1838380	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs4763004	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4763131	0.87[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4965015	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7314952	1.00[JPT][hapmap]
rs9668407	1.00[JPT][hapmap]
rs9668420	1.00[JPT][hapmap]
rs9668428	1.00[JPT][hapmap]
rs9669020	1.00[JPT][hapmap]
rs9669149	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9669794	1.00[JPT][hapmap]
rs9737644	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9739051	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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62402400-62403200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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