Variant report

Variant	rs72999197
Chromosome Location	chr3:146044864-146044865
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:146044616..146045587-chr3:146295200..146296047,4	MCF-7	breast:
2	chr3:145936384..145937370-chr3:146044670..146045567,4	MCF-7	breast:
3	chr3:145936462..145937370-chr3:146044619..146045821,9	MCF-7	breast:
4	chr3:145937350..145938198-chr3:146044684..146045576,2	K562	blood:
5	chr3:145783038..145783586-chr3:146044661..146045578,2	MCF-7	breast:
6	chr3:145938109..145938869-chr3:146044708..146045495,2	MCF-7	breast:
7	chr3:146044568..146045746-chr3:146099870..146100750,3	MCF-7	breast:
8	chr3:145940299..145941372-chr3:146044662..146045624,8	MCF-7	breast:
9	chr3:145907332..145908011-chr3:146044703..146045227,2	K562	blood:

No data

Extended variants
information (count: 94 )
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	1.00[EUR][1000 genomes]
rs41537446	1.00[EUR][1000 genomes]
rs56364069	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56945578	1.00[EUR][1000 genomes]
rs57016931	1.00[EUR][1000 genomes]
rs57202132	1.00[EUR][1000 genomes]
rs57555021	1.00[EUR][1000 genomes]
rs57702664	1.00[AMR][1000 genomes];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[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59001257	1.00[EUR][1000 genomes]
rs59060080	1.00[EUR][1000 genomes]
rs59125030	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59201889	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59202860	1.00[EUR][1000 genomes]
rs59652731	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60028092	1.00[AMR][1000 genomes];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[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6765013	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6766725	0.90[EUR][1000 genomes]
rs6767570	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6777637	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6777974	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72991486	0.90[EUR][1000 genomes]
rs72991490	0.90[EUR][1000 genomes]
rs72991492	0.90[EUR][1000 genomes]
rs72991494	0.90[EUR][1000 genomes]
rs72992903	1.00[EUR][1000 genomes]
rs72992908	1.00[EUR][1000 genomes]
rs72992924	1.00[EUR][1000 genomes]
rs72992931	1.00[EUR][1000 genomes]
rs72992934	1.00[EUR][1000 genomes]
rs72992963	1.00[EUR][1000 genomes]
rs72992964	1.00[EUR][1000 genomes]
rs72992966	1.00[EUR][1000 genomes]
rs72992968	1.00[EUR][1000 genomes]
rs72992969	1.00[EUR][1000 genomes]
rs72992975	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	1.00[EUR][1000 genomes]
rs72995025	1.00[EUR][1000 genomes]
rs72995029	1.00[EUR][1000 genomes]
rs72995034	1.00[EUR][1000 genomes]
rs72999169	1.00[EUR][1000 genomes]
rs72999182	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72999189	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73001103	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73001107	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73001112	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73001132	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73001133	1.00[AMR][1000 genomes];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	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];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[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7650651	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7651598	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7651977	1.00[EUR][1000 genomes]
rs7652262	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	nsv998388	chr3:145960954-146087749	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	esv3410778	chr3:146017303-146060390	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146043600-146050800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr3:146043600-146051000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr3:146044200-146045000	Enhancers	Aorta	Aorta
4	chr3:146044400-146045000	Enhancers	NHDF-Ad	bronchial
5	chr3:146044600-146045000	Enhancers	Liver	Liver
6	chr3:146044600-146045000	Enhancers	Ovary	ovary
7	chr3:146044600-146045000	Enhancers	A549	lung
8	chr3:146044600-146045000	Flanking Active TSS	Hela-S3	cervix
9	chr3:146044800-146045000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:146044800-146045200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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