Variant report

Variant	rs2220858
Chromosome Location	chr5:116632207-116632208
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10035146	0.82[EUR][1000 genomes]
rs10037418	0.82[EUR][1000 genomes]
rs10066055	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10068349	0.87[AFR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10068673	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10079309	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10080021	0.83[EUR][1000 genomes]
rs10085046	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10463690	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10478339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11241420	0.81[ASN][1000 genomes]
rs11957082	0.83[EUR][1000 genomes]
rs12652528	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13170803	0.86[EUR][1000 genomes]
rs13184380	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1353285	0.82[EUR][1000 genomes]
rs1389934	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1389935	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1494818	0.81[EUR][1000 genomes]
rs1494820	0.85[EUR][1000 genomes]
rs1494821	0.88[EUR][1000 genomes]
rs1494823	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1565889	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1565890	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1565892	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1908408	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1908409	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1976282	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2036024	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2900101	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34469130	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35793287	0.82[EUR][1000 genomes]
rs4331937	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4435900	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4642406	0.84[EUR][1000 genomes]
rs55813945	0.83[EUR][1000 genomes]
rs56020309	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs60269947	0.84[EUR][1000 genomes]
rs6595020	0.83[EUR][1000 genomes]
rs6595026	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6595028	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6862441	0.82[EUR][1000 genomes]
rs7702997	0.83[EUR][1000 genomes]
rs7703434	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7712165	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7714476	0.83[EUR][1000 genomes]
rs7729749	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7730432	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7732328	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7735145	0.87[ASN][1000 genomes]
rs7735868	0.87[ASN][1000 genomes]
rs7736463	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][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	nsv1015741	chr5:116525936-116665270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv599486	chr5:116607979-116669707	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116631200-116634600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:116631800-116633600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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