Variant report

Variant	rs73183661
Chromosome Location	chr12:103488065-103488066
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12312776	1.00[ASN][1000 genomes]
rs12313548	1.00[ASN][1000 genomes]
rs12318722	1.00[ASN][1000 genomes]
rs12318972	1.00[ASN][1000 genomes]
rs1543127	1.00[EUR][1000 genomes]
rs17033429	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17033447	1.00[ASN][1000 genomes]
rs73176076	0.94[EUR][1000 genomes]
rs73176078	1.00[EUR][1000 genomes]
rs73176079	1.00[EUR][1000 genomes]
rs73176080	1.00[EUR][1000 genomes]
rs73176081	0.94[EUR][1000 genomes]
rs73176082	1.00[EUR][1000 genomes]
rs73179703	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73179704	1.00[EUR][1000 genomes]
rs73183634	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73183635	1.00[EUR][1000 genomes]
rs73183647	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73183649	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73183651	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73183654	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73183655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183658	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183659	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183660	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183663	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183668	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183672	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183673	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183674	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183675	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183676	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv832501	chr12:103463927-103648825	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103486600-103489400	Enhancers	Fetal Intestine Large	intestine
2	chr12:103486600-103489400	Enhancers	Fetal Intestine Small	intestine
3	chr12:103486800-103488600	Enhancers	Stomach Mucosa	stomach
4	chr12:103487800-103488200	Enhancers	Liver	Liver
5	chr12:103487800-103488200	Flanking Active TSS	Duodenum Mucosa	Duodenum
6	chr12:103488000-103488400	Enhancers	Rectal Mucosa Donor 31	rectum

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