Variant report

Variant	rs11694699
Chromosome Location	chr2:182984631-182984632
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10181222	0.80[EUR][1000 genomes]
rs10181420	0.80[EUR][1000 genomes]
rs10193834	0.80[EUR][1000 genomes]
rs10197864	0.80[EUR][1000 genomes]
rs10205020	0.80[EUR][1000 genomes]
rs10451546	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11686047	0.80[EUR][1000 genomes]
rs11899083	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12473915	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12474446	0.81[EUR][1000 genomes]
rs13398100	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1432524	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1515897	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16822592	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17648960	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1878093	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1882212	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1921149	0.80[EUR][1000 genomes]
rs1921150	0.80[EUR][1000 genomes]
rs1921151	0.80[EUR][1000 genomes]
rs1921152	0.80[EUR][1000 genomes]
rs2163697	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2195879	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3731689	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4666813	0.80[EUR][1000 genomes]
rs4666814	0.80[EUR][1000 genomes]
rs60286884	0.80[EUR][1000 genomes]
rs6433954	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6732308	0.80[EUR][1000 genomes]
rs6744499	0.80[EUR][1000 genomes]
rs6760627	0.80[EUR][1000 genomes]
rs6760977	0.80[EUR][1000 genomes]
rs73040730	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7558141	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7558159	0.80[EUR][1000 genomes]
rs7567207	0.80[EUR][1000 genomes]
rs7593639	0.80[EUR][1000 genomes]
rs7593912	0.80[EUR][1000 genomes]
rs7606356	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs768742	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs998617	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][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	nsv875477	chr2:182938377-183086478	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv875478	chr2:182960289-182998122	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr2:182966800-182996400	Weak transcription	Fetal Thymus	thymus

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