Variant report

Variant	rs9693826
Chromosome Location	chr8:20646927-20646928
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10104667	0.87[ASN][1000 genomes]
rs10111144	0.80[ASN][1000 genomes]
rs10113832	0.91[ASN][1000 genomes]
rs11204131	0.82[ASN][1000 genomes]
rs1159219	0.86[ASN][1000 genomes]
rs2410665	0.81[ASN][1000 genomes]
rs2410666	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2597418	0.91[AFR][1000 genomes]
rs2616141	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2616142	0.86[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2616257	0.84[ASN][1000 genomes]
rs28507679	0.91[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs35665887	0.81[ASN][1000 genomes]
rs4352868	0.80[EUR][1000 genomes]
rs59497697	0.86[ASN][1000 genomes]
rs7011200	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	esv2761417	chr8:20523767-20669443	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1033319	chr8:20606592-20718378	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv831257	chr8:20610436-20767433	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv1021366	chr8:20624387-20726669	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv539525	chr8:20624387-20726669	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20642200-20647400	Enhancers	Fetal Heart	heart
2	chr8:20644200-20651000	Weak transcription	Right Atrium	heart
3	chr8:20645200-20647200	Enhancers	Fetal Stomach	stomach
4	chr8:20645600-20647200	Enhancers	Fetal Brain Female	brain
5	chr8:20646600-20647000	Enhancers	Fetal Lung	lung
6	chr8:20646600-20647400	Enhancers	Fetal Brain Male	brain

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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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