Variant report

Variant	rs73683015
Chromosome Location	chr8:63112259-63112260
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs56158875	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56859587	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57963179	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58165428	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58819717	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59574888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59720904	1.00[AMR][1000 genomes]
rs59899302	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60198522	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60249107	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60425003	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60453695	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60926640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61190800	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61575867	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683011	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683013	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683014	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683019	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683020	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683021	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683022	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683024	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683025	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683026	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683027	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683028	0.98[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016883	chr8:63110741-63171354	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63111400-63112600	Enhancers	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links