Variant report

Variant	rs73867523
Chromosome Location	chr3:145989366-145989367
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	0.90[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[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	0.90[EUR][1000 genomes]
rs6767570	1.00[EUR][1000 genomes]
rs6777637	1.00[EUR][1000 genomes]
rs6777974	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	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	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73867521	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];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	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	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	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
3	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
4	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

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145983800-145998800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:145984600-145990000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:145987000-145991800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:145987000-145992000	Weak transcription	Muscle Satellite Cultured Cells	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links