Variant report

Variant	rs72992908
Chromosome Location	chr3:145951841-145951842
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs16858173	1.00[EUR][1000 genomes]
rs16858176	1.00[EUR][1000 genomes]
rs16858179	1.00[EUR][1000 genomes]
rs41358845	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41537446	1.00[EUR][1000 genomes]
rs56364069	0.90[EUR][1000 genomes]
rs56945578	1.00[EUR][1000 genomes]
rs57016931	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57202132	1.00[EUR][1000 genomes]
rs57555021	1.00[EUR][1000 genomes]
rs57702664	1.00[EUR][1000 genomes]
rs57852021	1.00[EUR][1000 genomes]
rs58284373	1.00[EUR][1000 genomes]
rs58434679	1.00[EUR][1000 genomes]
rs58523990	1.00[EUR][1000 genomes]
rs59001257	1.00[EUR][1000 genomes]
rs59060080	1.00[EUR][1000 genomes]
rs59125030	1.00[EUR][1000 genomes]
rs59201889	1.00[EUR][1000 genomes]
rs59202860	1.00[EUR][1000 genomes]
rs59652731	1.00[EUR][1000 genomes]
rs60028092	1.00[EUR][1000 genomes]
rs60271422	1.00[EUR][1000 genomes]
rs60489907	1.00[EUR][1000 genomes]
rs60843942	1.00[EUR][1000 genomes]
rs60922478	1.00[EUR][1000 genomes]
rs61440265	1.00[EUR][1000 genomes]
rs6440427	1.00[EUR][1000 genomes]
rs6765013	1.00[EUR][1000 genomes]
rs6766725	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6767570	1.00[EUR][1000 genomes]
rs6777637	1.00[EUR][1000 genomes]
rs6777974	1.00[EUR][1000 genomes]
rs72991486	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72991490	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72991492	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72991494	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72992903	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992924	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992931	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992934	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992963	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992964	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992966	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992968	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992969	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992975	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72992981	1.00[EUR][1000 genomes]
rs72992986	1.00[EUR][1000 genomes]
rs72992988	1.00[EUR][1000 genomes]
rs72992989	1.00[EUR][1000 genomes]
rs72993002	1.00[EUR][1000 genomes]
rs72995008	1.00[EUR][1000 genomes]
rs72995010	1.00[EUR][1000 genomes]
rs72995012	1.00[EUR][1000 genomes]
rs72995014	1.00[EUR][1000 genomes]
rs72995019	1.00[EUR][1000 genomes]
rs72995022	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72995025	1.00[EUR][1000 genomes]
rs72995029	1.00[EUR][1000 genomes]
rs72995034	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72999169	1.00[EUR][1000 genomes]
rs72999182	1.00[EUR][1000 genomes]
rs72999189	1.00[EUR][1000 genomes]
rs72999197	1.00[EUR][1000 genomes]
rs73001103	1.00[EUR][1000 genomes]
rs73001107	1.00[EUR][1000 genomes]
rs73001112	1.00[EUR][1000 genomes]
rs73001132	1.00[EUR][1000 genomes]
rs73001133	1.00[EUR][1000 genomes]
rs73865394	1.00[EUR][1000 genomes]
rs73867504	1.00[EUR][1000 genomes]
rs73867507	1.00[EUR][1000 genomes]
rs73867511	1.00[EUR][1000 genomes]
rs73867513	0.90[EUR][1000 genomes]
rs73867518	1.00[EUR][1000 genomes]
rs73867520	1.00[EUR][1000 genomes]
rs73867521	1.00[EUR][1000 genomes]
rs73867523	1.00[EUR][1000 genomes]
rs7610563	1.00[EUR][1000 genomes]
rs7629318	1.00[EUR][1000 genomes]
rs7630137	1.00[EUR][1000 genomes]
rs7630230	1.00[EUR][1000 genomes]
rs7632298	1.00[EUR][1000 genomes]
rs7642529	0.90[EUR][1000 genomes]
rs7650158	1.00[EUR][1000 genomes]
rs7650651	1.00[EUR][1000 genomes]
rs7651598	1.00[EUR][1000 genomes]
rs7651977	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7652262	1.00[EUR][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	nsv877614	chr3:145903426-146025896	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
2	nsv877615	chr3:145910430-145988231	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv877616	chr3:145921954-145983688	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv3333601	chr3:145940702-146068210	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	esv3416330	chr3:145941029-146068457	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv3452197	chr3:145950303-145974111	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
7	esv3333990	chr3:145950303-145982133	ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145925400-145952800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr3:145934600-145952200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr3:145940600-145953000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr3:145940600-145953600	Weak transcription	NHDF-Ad	bronchial
5	chr3:145941600-145952200	Weak transcription	Left Ventricle	heart
6	chr3:145941600-145952600	Weak transcription	Fetal Intestine Small	intestine
7	chr3:145941600-145954000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr3:145942200-145953400	Weak transcription	HUVEC	blood vessel
9	chr3:145945200-145959800	Weak transcription	Ovary	ovary
10	chr3:145946000-145952400	Weak transcription	Fetal Stomach	stomach
11	chr3:145946200-145952600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:145946400-145953000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr3:145947200-145953000	Weak transcription	Adipose Nuclei	Adipose
14	chr3:145947400-145953200	Weak transcription	Fetal Intestine Large	intestine
15	chr3:145948000-145967800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr3:145948600-145952000	Weak transcription	Aorta	Aorta
17	chr3:145950800-145953000	Weak transcription	Fetal Lung	lung
18	chr3:145951000-145953000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr3:145951600-145952200	Enhancers	Liver	Liver

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