Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10133349	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10140107	0.87[ASN][1000 genomes]
rs1031787	0.90[ASN][1000 genomes]
rs11159633	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11844860	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12431743	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12878411	0.93[ASN][1000 genomes]
rs12879881	0.91[ASN][1000 genomes]
rs12881717	0.94[ASN][1000 genomes]
rs1462339	0.91[ASN][1000 genomes]
rs3001377	0.89[ASN][1000 genomes]
rs6574776	0.90[ASN][1000 genomes]
rs6574777	0.90[ASN][1000 genomes]
rs7148526	0.93[ASN][1000 genomes]
rs7157884	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs734656	0.97[ASN][1000 genomes]
rs744740	0.96[ASN][1000 genomes]
rs7493899	0.90[ASN][1000 genomes]
rs8004689	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs8004742	0.90[ASN][1000 genomes]
rs8004749	0.90[ASN][1000 genomes]

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	nsv85516	chr14:84664110-84671508	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	n/a
2	nsv976854	chr14:84667225-84675082	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84666400-84669600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:84668800-84669600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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