Variant report

Variant	rs57126669
Chromosome Location	chr2:185621860-185621861
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11883625	1.00[EUR][1000 genomes]
rs11891366	1.00[EUR][1000 genomes]
rs11898003	1.00[EUR][1000 genomes]
rs11898500	1.00[EUR][1000 genomes]
rs11899942	1.00[EUR][1000 genomes]
rs13384922	1.00[EUR][1000 genomes]
rs13417933	1.00[EUR][1000 genomes]
rs1365719	1.00[AMR][1000 genomes]
rs359883	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs359897	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs384591	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs406498	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4618009	1.00[EUR][1000 genomes]
rs56200326	1.00[EUR][1000 genomes]
rs59038604	1.00[EUR][1000 genomes]
rs59102345	1.00[EUR][1000 genomes]
rs59318193	1.00[EUR][1000 genomes]
rs60535211	1.00[EUR][1000 genomes]
rs61400218	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6760206	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73043271	1.00[EUR][1000 genomes]
rs73978033	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73978034	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73978036	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73978037	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73978039	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73978042	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73978079	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73978095	1.00[EUR][1000 genomes]
rs73978098	1.00[EUR][1000 genomes]
rs73978101	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73980304	1.00[EUR][1000 genomes]
rs73980313	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73980315	1.00[EUR][1000 genomes]
rs73980325	1.00[EUR][1000 genomes]
rs73980326	1.00[EUR][1000 genomes]
rs73980329	1.00[EUR][1000 genomes]
rs7579459	1.00[EUR][1000 genomes]
rs7585984	1.00[EUR][1000 genomes]
rs7601869	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532412	chr2:185347334-186108701	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv834484	chr2:185550006-185762728	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:185621200-185622800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:185621400-185622200	Enhancers	Muscle Satellite Cultured Cells	--
3	chr2:185621800-185622400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links