Variant report

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10178473	0.82[ASN][1000 genomes]
rs10178858	0.82[ASN][1000 genomes]
rs10178916	0.82[ASN][1000 genomes]
rs10179500	0.81[ASN][1000 genomes]
rs10182017	0.82[ASN][1000 genomes]
rs10182353	0.80[ASN][1000 genomes]
rs10202536	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13395965	0.82[ASN][1000 genomes]
rs13396065	0.82[ASN][1000 genomes]
rs13396537	0.82[ASN][1000 genomes]
rs13421345	0.82[ASN][1000 genomes]
rs1438042	0.82[ASN][1000 genomes]
rs28380215	0.80[ASN][1000 genomes]
rs4297923	0.83[ASN][1000 genomes]
rs4464321	0.81[ASN][1000 genomes]
rs56314683	0.82[ASN][1000 genomes]
rs56690966	0.82[ASN][1000 genomes]
rs56760518	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57342997	0.82[ASN][1000 genomes]
rs62183048	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62183050	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62183051	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6433694	0.83[ASN][1000 genomes]
rs6709966	0.82[ASN][1000 genomes]
rs6718100	0.81[ASN][1000 genomes]
rs6718657	0.83[ASN][1000 genomes]
rs6718860	0.82[ASN][1000 genomes]
rs6718993	0.83[ASN][1000 genomes]
rs6726253	0.83[ASN][1000 genomes]
rs6726502	0.82[ASN][1000 genomes]
rs6733980	0.81[ASN][1000 genomes]
rs6737872	0.81[ASN][1000 genomes]
rs6743821	0.82[ASN][1000 genomes]
rs6751656	0.82[ASN][1000 genomes]
rs6752264	0.82[ASN][1000 genomes]
rs6758508	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999086	chr2:178262348-178773585	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv536055	chr2:178262348-178773585	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv583690	chr2:178638381-178712283	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 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	chr2:178649400-178662000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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