Variant report

Variant	rs2583675
Chromosome Location	chr8:20689576-20689577
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11989998	1.00[EUR][1000 genomes]
rs11990001	1.00[EUR][1000 genomes]
rs11991753	1.00[EUR][1000 genomes]
rs1441796	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1441798	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17092970	1.00[EUR][1000 genomes]
rs17093103	1.00[EUR][1000 genomes]
rs17093105	1.00[EUR][1000 genomes]
rs17093107	1.00[EUR][1000 genomes]
rs17093145	1.00[EUR][1000 genomes]
rs1946955	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2583688	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28416913	1.00[EUR][1000 genomes]
rs28447174	1.00[EUR][1000 genomes]
rs28465358	1.00[EUR][1000 genomes]
rs28639666	1.00[EUR][1000 genomes]
rs57509222	1.00[EUR][1000 genomes]
rs59265254	1.00[EUR][1000 genomes]
rs7016713	1.00[EUR][1000 genomes]
rs7017521	1.00[EUR][1000 genomes]
rs73625285	1.00[EUR][1000 genomes]
rs73668013	1.00[EUR][1000 genomes]
rs73668122	1.00[EUR][1000 genomes]
rs7845145	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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	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
4	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
5	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
6	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
7	nsv1020160	chr8:20652610-20825810	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv539526	chr8:20652610-20825810	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1024612	chr8:20665835-20837761	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv539527	chr8:20665835-20837761	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	esv1803225	chr8:20684287-20693912	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	nsv525207	chr8:20685467-20691295	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20684400-20689800	Weak transcription	Fetal Heart	heart
2	chr8:20689400-20689600	Enhancers	Placenta	Placenta
3	chr8:20689400-20690200	Enhancers	Ovary	ovary
4	chr8:20689400-20690600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:20689400-20690600	Enhancers	Liver	Liver
6	chr8:20689400-20690600	Enhancers	Fetal Lung	lung
7	chr8:20689400-20690800	Enhancers	Fetal Stomach	stomach
8	chr8:20689400-20691000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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