Variant report

Variant	rs61562183
Chromosome Location	chr8:58186465-58186466
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs17216711	0.92[AFR][1000 genomes]
rs17805380	0.92[AFR][1000 genomes]
rs17805439	0.92[AFR][1000 genomes]
rs17816781	0.97[AFR][1000 genomes]
rs3814486	0.90[AFR][1000 genomes]
rs55787104	0.90[AFR][1000 genomes]
rs56255635	0.94[AFR][1000 genomes]
rs56350499	0.94[AFR][1000 genomes]
rs56740825	0.92[AFR][1000 genomes]
rs57131327	0.89[AFR][1000 genomes]
rs57261109	0.90[AFR][1000 genomes]
rs57669205	0.92[AFR][1000 genomes]
rs57942497	0.92[AFR][1000 genomes]
rs58053450	0.92[AFR][1000 genomes]
rs58251024	0.92[AFR][1000 genomes]
rs58559296	0.92[AFR][1000 genomes]
rs58947041	0.93[AFR][1000 genomes]
rs59071610	0.97[AFR][1000 genomes]
rs59549824	0.93[AFR][1000 genomes]
rs59873610	0.92[AFR][1000 genomes]
rs60454728	0.92[AFR][1000 genomes]
rs60651159	0.92[AFR][1000 genomes]
rs61212428	0.92[AFR][1000 genomes]
rs61733801	0.94[AFR][1000 genomes]
rs61998258	0.94[AFR][1000 genomes]
rs61998259	0.94[AFR][1000 genomes]
rs66480865	0.97[AFR][1000 genomes]
rs66509078	0.92[AFR][1000 genomes]
rs66676208	0.89[AFR][1000 genomes]
rs66796009	0.92[AFR][1000 genomes]
rs66886949	0.97[AFR][1000 genomes]
rs67039591	0.92[AFR][1000 genomes]
rs67042991	0.94[AFR][1000 genomes]
rs67105789	0.94[AFR][1000 genomes]
rs67243305	0.92[AFR][1000 genomes]
rs67630725	0.97[AFR][1000 genomes]
rs67677367	0.92[AFR][1000 genomes]
rs67886764	0.97[AFR][1000 genomes]
rs67895971	0.92[AFR][1000 genomes]
rs68076606	0.94[AFR][1000 genomes]
rs6989060	0.97[AFR][1000 genomes]
rs7003285	0.92[AFR][1000 genomes]
rs7006539	0.84[AFR][1000 genomes]
rs7007128	0.97[AFR][1000 genomes]
rs72650885	0.92[AFR][1000 genomes]
rs72650900	0.97[AFR][1000 genomes]
rs72652908	0.93[AFR][1000 genomes]
rs73607868	0.92[AFR][1000 genomes]
rs73607869	0.88[AFR][1000 genomes]
rs73607871	0.92[AFR][1000 genomes]
rs73607874	0.92[AFR][1000 genomes]
rs73607875	0.92[AFR][1000 genomes]
rs73609760	0.94[AFR][1000 genomes]
rs73609762	0.94[AFR][1000 genomes]
rs73609764	0.94[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758161	chr8:57930392-58474449	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv2759618	chr8:57930392-58474449	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv533217	chr8:57991065-58789001	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	esv12840	chr8:58046936-58196713	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv3432915	chr8:58055026-58271178	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1793550	chr8:58063507-58215957	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv1804272	chr8:58063507-58215957	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	esv1814738	chr8:58063507-58215957	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv428200	chr8:58063507-58215957	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv831321	chr8:58086885-58237744	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	esv12323	chr8:58114793-58199474	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv981943	chr8:58174408-58222589	Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	esv1828349	chr8:58175232-58198324	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	esv1830364	chr8:58175432-58198163	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv8353	chr8:58179206-58188314	Enhancers Flanking Active TSS	TF binding region	1 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	chr8:58185600-58187200	Enhancers	Fetal Lung	lung
2	chr8:58185800-58186600	Enhancers	HepG2	liver

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