Variant report

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

rs_ID	r²[population]
rs1036609	0.81[ASN][1000 genomes]
rs10496628	0.80[CEU][hapmap];0.84[GIH][hapmap]
rs1213938	0.81[CHB][hapmap]
rs1213942	0.81[CHB][hapmap]
rs1213945	0.81[CHB][hapmap];0.80[CHD][hapmap];0.81[MKK][hapmap]
rs1213946	0.81[CHB][hapmap];0.80[CHD][hapmap]
rs1213948	0.81[CHB][hapmap]
rs1213950	0.86[CHB][hapmap];0.84[GIH][hapmap];0.82[LWK][hapmap];0.86[MKK][hapmap]
rs1213956	0.86[CHB][hapmap];0.81[GIH][hapmap]
rs1213958	0.81[CHB][hapmap]
rs1213962	0.82[CHB][hapmap]
rs1228168	0.86[CHB][hapmap]
rs1347876	0.93[CHB][hapmap];0.88[CHD][hapmap];0.84[GIH][hapmap];0.90[JPT][hapmap];0.84[MEX][hapmap];0.81[ASN][1000 genomes]
rs17010766	0.86[CHB][hapmap]
rs17010827	0.86[CHB][hapmap]
rs17010848	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17010876	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17278676	1.00[CHB][hapmap];0.96[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.86[ASN][1000 genomes]
rs17391285	0.91[CEU][hapmap];0.94[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap]
rs1816698	0.86[CHB][hapmap];0.84[GIH][hapmap];0.82[LWK][hapmap];0.86[MKK][hapmap]
rs1898788	0.86[CHB][hapmap]
rs4450605	0.82[CEU][hapmap]
rs7567584	0.86[CHB][hapmap]
rs7577916	0.89[GIH][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	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:124878400-124880800	Enhancers	Fetal Lung	lung

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