Variant report

Variant	rs9650051
Chromosome Location	chr8:114370787-114370788
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10087093	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1017829	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11778755	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13249480	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13270413	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1402943	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1478678	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1480462	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1522058	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1522065	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17607120	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1904217	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1904218	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2030507	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2356203	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs2356204	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2883875	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4242551	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4565484	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6469452	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs750262	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7824290	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7825515	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7833634	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7834106	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7836578	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7843570	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs899831	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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	esv2754581	chr8:114029421-114419106	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv817379	chr8:114338391-115011632	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2754463	chr8:114353649-114501547	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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