Variant report

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

rs_ID	r²[population]
rs10877781	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11174276	0.90[CHB][hapmap];0.88[YRI][hapmap]
rs1121705	1.00[JPT][hapmap]
rs11609846	0.84[ASN][1000 genomes]
rs1371918	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
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	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4763004	0.95[ASN][1000 genomes]
rs4965015	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][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[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9669794	1.00[JPT][hapmap]
rs9737644	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:0 , 50 per page) page:

No data

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