Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10095221	0.83[AFR][1000 genomes]
rs10095647	0.84[EUR][1000 genomes]
rs10099895	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10106856	0.83[EUR][1000 genomes]
rs11782332	0.81[AMR][1000 genomes]
rs11784050	1.00[ASN][1000 genomes]
rs13258690	1.00[ASN][1000 genomes]
rs13258830	0.85[AFR][1000 genomes]
rs13272568	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13274461	1.00[ASN][1000 genomes]
rs13278866	0.97[ASN][1000 genomes]
rs13281068	1.00[ASN][1000 genomes]
rs1383837	0.80[EUR][1000 genomes]
rs1481513	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17483138	1.00[ASN][1000 genomes]
rs2368503	1.00[ASN][1000 genomes]
rs4308718	0.97[ASN][1000 genomes]
rs62510275	1.00[ASN][1000 genomes]
rs6473090	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6988252	0.82[EUR][1000 genomes]
rs6989455	0.83[EUR][1000 genomes]
rs6991500	1.00[ASN][1000 genomes]
rs957280	0.90[AFR][1000 genomes];1.00[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	nsv526123	chr8:79008608-79046492	Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv525612	chr8:79008608-79046695	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:79025800-79026800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr8:79026000-79026600	Weak transcription	NHEK	skin
3	chr8:79026000-79027000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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