Variant report

Variant	rs11486326
Chromosome Location	chr13:92610311-92610312
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12184638	1.00[YRI][hapmap]
rs13379011	0.82[YRI][hapmap]
rs1409501	1.00[EUR][1000 genomes]
rs1409502	1.00[EUR][1000 genomes]
rs1411743	1.00[EUR][1000 genomes]
rs16946937	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58772509	1.00[EUR][1000 genomes]
rs58841974	1.00[EUR][1000 genomes]
rs61049774	1.00[EUR][1000 genomes]
rs73607673	1.00[AMR][1000 genomes]
rs73607679	1.00[AMR][1000 genomes]
rs73607684	1.00[AMR][1000 genomes]
rs73607687	1.00[AMR][1000 genomes]
rs73607696	1.00[AMR][1000 genomes]
rs73620031	1.00[EUR][1000 genomes]
rs73623542	1.00[EUR][1000 genomes]
rs7997781	1.00[EUR][1000 genomes]
rs9583968	1.00[AMR][1000 genomes]
rs9589367	1.00[AMR][1000 genomes]
rs9589371	1.00[YRI][hapmap]
rs9589374	1.00[YRI][hapmap]
rs9589404	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9589405	1.00[EUR][1000 genomes]
rs9589408	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9589421	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3378326	chr13:92445514-92816367	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv900885	chr13:92561714-92621620	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv900886	chr13:92576149-92626399	Enhancers ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv562722	chr13:92607374-92733984	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links