Variant report

Variant	rs4762752
Chromosome Location	chr12:20543299-20543300
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10734701	1.00[ASN][1000 genomes]
rs10743369	1.00[ASN][1000 genomes]
rs10770655	1.00[ASN][1000 genomes]
rs10841515	1.00[ASN][1000 genomes]
rs12370696	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1373572	1.00[ASN][1000 genomes]
rs1373573	1.00[ASN][1000 genomes]
rs1444631	1.00[ASN][1000 genomes]
rs1444633	1.00[ASN][1000 genomes]
rs1530445	1.00[ASN][1000 genomes]
rs1822751	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1822752	1.00[ASN][1000 genomes]
rs1822753	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1822756	1.00[ASN][1000 genomes]
rs2417850	1.00[ASN][1000 genomes]
rs3919734	1.00[ASN][1000 genomes]
rs4762950	0.83[EUR][1000 genomes]
rs4762951	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5007546	1.00[ASN][1000 genomes]
rs5014038	1.00[ASN][1000 genomes]
rs7133921	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7299430	1.00[ASN][1000 genomes]
rs7964191	1.00[ASN][1000 genomes]
rs7964703	1.00[ASN][1000 genomes]
rs7979838	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048067	chr12:20363755-20874845	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv541408	chr12:20363755-20874845	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1046870	chr12:20509914-20711535	Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
4	nsv541409	chr12:20509914-20711535	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
5	nsv1042315	chr12:20531641-20629866	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20533200-20544800	Weak transcription	Right Atrium	heart
2	chr12:20538200-20550400	Weak transcription	HUVEC	blood vessel
3	chr12:20538200-20558000	Weak transcription	Left Ventricle	heart
4	chr12:20540200-20544000	Enhancers	Colon Smooth Muscle	Colon
5	chr12:20540600-20546200	Enhancers	Fetal Intestine Large	intestine
6	chr12:20541600-20543600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr12:20541600-20544000	Enhancers	Fetal Heart	heart
8	chr12:20542000-20543400	Enhancers	Fetal Intestine Small	intestine
9	chr12:20542000-20543400	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr12:20542000-20543400	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr12:20542000-20544000	Enhancers	Ovary	ovary
12	chr12:20542000-20544200	Enhancers	Adipose Nuclei	Adipose
13	chr12:20542200-20544200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr12:20542400-20543600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr12:20542400-20545600	Weak transcription	Right Ventricle	heart
16	chr12:20542600-20566200	Weak transcription	Aorta	Aorta
17	chr12:20542800-20543800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr12:20542800-20544000	Enhancers	Duodenum Mucosa	Duodenum
19	chr12:20543000-20543600	Enhancers	Colonic Mucosa	Colon
20	chr12:20543000-20544000	Enhancers	NHDF-Ad	bronchial
21	chr12:20543000-20547000	Weak transcription	Small Intestine	intestine
22	chr12:20543000-20549200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr12:20543000-20551000	Weak transcription	A549	lung
24	chr12:20543200-20544000	Enhancers	Osteobl	bone
25	chr12:20543200-20544600	Weak transcription	Hela-S3	cervix

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