Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10485437	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1120258	0.82[AMR][1000 genomes]
rs11751644	0.83[AMR][1000 genomes]
rs13191427	0.91[ASN][1000 genomes]
rs13199576	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13201188	0.95[ASN][1000 genomes]
rs13204176	0.94[ASN][1000 genomes]
rs13208434	0.83[AMR][1000 genomes]
rs13210533	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13210818	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13215030	0.95[ASN][1000 genomes]
rs13216650	0.91[ASN][1000 genomes]
rs13217051	0.82[AMR][1000 genomes]
rs16900333	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17200696	0.83[AMR][1000 genomes]
rs1916767	0.83[AMR][1000 genomes]
rs1932615	0.92[ASN][1000 genomes]
rs2184723	0.95[ASN][1000 genomes]
rs62416371	0.83[AMR][1000 genomes]
rs62418573	0.80[AMR][1000 genomes]
rs6936651	0.83[AMR][1000 genomes]
rs73458284	0.80[AMR][1000 genomes]
rs7754330	0.83[AMR][1000 genomes]
rs7760666	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9294813	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9446064	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9446067	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9454643	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9454645	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470831	chr6:69581991-69654650	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv886136	chr6:69598297-69654650	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv525968	chr6:69618480-69638504	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv519494	chr6:69619007-69638504	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3339572	chr6:69620331-69624529	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69621200-69622000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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