Variant report

Variant	rs7001191
Chromosome Location	chr8:60639103-60639104
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs16925218	1.00[EUR][1000 genomes]
rs4351408	1.00[EUR][1000 genomes]
rs56055752	1.00[EUR][1000 genomes]
rs58334138	1.00[EUR][1000 genomes]
rs60478918	1.00[EUR][1000 genomes]
rs73251501	1.00[EUR][1000 genomes]
rs73682834	1.00[EUR][1000 genomes]
rs907207	0.86[AFR][1000 genomes]
rs907208	0.86[AFR][1000 genomes]
rs9657028	1.00[EUR][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	nsv1030564	chr8:60445016-60752655	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv539630	chr8:60445016-60752655	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr8:60638800-60639800	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:60639000-60639800	Enhancers	Primary B cells from cord blood	blood

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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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