Variant report

Variant	rs6586961
Chromosome Location	chr8:20880887-20880888
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11994276	0.82[AFR][1000 genomes]
rs13268443	1.00[AFR][1000 genomes]
rs41359246	1.00[AMR][1000 genomes]
rs58705442	1.00[AMR][1000 genomes]
rs6421421	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6421422	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6586956	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6586957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6586958	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6586959	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6988856	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6996350	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7388658	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7459961	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032450	chr8:20514995-21033577	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv539524	chr8:20514995-21033577	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1034265	chr8:20742935-21152545	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv539528	chr8:20742935-21152545	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv831258	chr8:20754932-20940380	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1028279	chr8:20843801-20930959	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20879000-20881200	Enhancers	Primary T cells from cord blood	blood
2	chr8:20880600-20881400	Enhancers	GM12878-XiMat	blood
3	chr8:20880800-20881000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr8:20880800-20881000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:20880800-20881200	Enhancers	Primary B cells from peripheral 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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