Variant report

Variant	rs8048291
Chromosome Location	chr16:59375465-59375466
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10492916	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10492917	0.91[ASN][1000 genomes]
rs11865643	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12102966	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13331749	0.92[ASN][1000 genomes]
rs13336506	0.92[ASN][1000 genomes]
rs17185925	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17185932	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17185953	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17185988	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17186051	0.85[ASN][1000 genomes]
rs17258122	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17258129	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17258157	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17258178	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17258185	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17258247	0.92[ASN][1000 genomes]
rs1828342	0.85[ASN][1000 genomes]
rs1978488	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28413921	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28815512	0.87[ASN][1000 genomes]
rs57159649	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57452945	0.92[ASN][1000 genomes]
rs59292600	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7185818	0.92[ASN][1000 genomes]
rs7188192	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7203225	0.92[ASN][1000 genomes]
rs73555951	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73563808	0.87[ASN][1000 genomes]
rs8044360	0.92[ASN][1000 genomes]
rs8060477	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9928215	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9939007	0.92[ASN][1000 genomes]
rs9939608	0.92[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	nsv833249	chr16:59282950-59461023	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv906745	chr16:59323025-59408342	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv906746	chr16:59323025-59423982	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	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	chr16:59375000-59375600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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