Variant report

Variant	rs7004583
Chromosome Location	chr8:20534046-20534047
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11986412	1.00[EUR][1000 genomes]
rs17092939	1.00[EUR][1000 genomes]
rs17092949	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17092968	1.00[EUR][1000 genomes]
rs17092979	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17093157	1.00[EUR][1000 genomes]
rs17093167	1.00[EUR][1000 genomes]
rs17093176	1.00[EUR][1000 genomes]
rs17116648	1.00[EUR][1000 genomes]
rs60973888	1.00[EUR][1000 genomes]
rs6987269	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6993881	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73667854	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73667857	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73667858	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73667859	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73667860	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73667873	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73668005	1.00[EUR][1000 genomes]
rs73668006	1.00[EUR][1000 genomes]
rs73668007	1.00[EUR][1000 genomes]
rs7815723	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7841702	0.92[AFR][1000 genomes];1.00[EUR][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	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv530877	chr8:19873053-20593254	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1027535	chr8:20506377-20613664	Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20528000-20535000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:20531200-20535400	Weak transcription	Liver	Liver
3	chr8:20531200-20535600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:20533800-20537000	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr8:20534000-20534800	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr8:20534000-20536200	Enhancers	Colonic Mucosa	Colon

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