Variant report

Variant	rs6656214
Chromosome Location	chr1:217281837-217281838
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1166347	0.96[ASN][1000 genomes]
rs1166350	1.00[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs1166351	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1318282	0.94[ASN][1000 genomes]
rs1354221	1.00[CEU][hapmap];0.91[JPT][hapmap]
rs1502357	0.89[CEU][hapmap];0.96[CHB][hapmap];0.81[JPT][hapmap];0.94[ASN][1000 genomes]
rs2252089	0.95[CHB][hapmap];0.86[JPT][hapmap];0.94[ASN][1000 genomes]
rs2789579	0.94[ASN][1000 genomes]
rs61066191	0.96[ASN][1000 genomes]
rs6682972	1.00[CHB][hapmap];0.96[JPT][hapmap];0.95[ASN][1000 genomes]
rs830310	0.95[ASN][1000 genomes]
rs905292	0.94[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428610	chr1:217143317-217307243	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	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	chr1:217280000-217283200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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