Variant report

Variant	rs11608539
Chromosome Location	chr12:86321862-86321863
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10082857	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10779220	0.92[ASN][1000 genomes]
rs10779224	0.82[EUR][1000 genomes]
rs10863111	0.92[ASN][1000 genomes]
rs10863112	0.92[ASN][1000 genomes]
rs10863113	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10863114	0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs10863124	0.92[ASN][1000 genomes]
rs11117115	0.92[ASN][1000 genomes]
rs11117118	0.92[ASN][1000 genomes]
rs11117122	0.92[ASN][1000 genomes]
rs11117124	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11117129	0.92[ASN][1000 genomes]
rs11117148	0.80[EUR][1000 genomes]
rs11611607	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11615948	0.95[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11615953	0.82[CEU][hapmap]
rs17354637	0.92[ASN][1000 genomes]
rs4919774	0.92[ASN][1000 genomes]
rs61929393	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61929394	0.92[ASN][1000 genomes]
rs61929395	0.92[ASN][1000 genomes]
rs7135154	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7136221	0.80[EUR][1000 genomes]
rs7303256	0.92[ASN][1000 genomes]
rs7307686	0.80[EUR][1000 genomes]
rs73176252	0.92[ASN][1000 genomes]
rs73177167	0.84[ASN][1000 genomes]
rs73177169	0.84[ASN][1000 genomes]
rs73177179	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7485853	0.80[EUR][1000 genomes]
rs7966131	0.81[YRI][hapmap];0.92[ASN][1000 genomes]
rs7972773	0.92[ASN][1000 genomes]
rs7973694	0.92[ASN][1000 genomes]
rs7975310	0.92[ASN][1000 genomes]
rs7976573	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9651977	0.96[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9706029	0.84[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv1797806	chr12:86198935-86425608	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv559667	chr12:86318004-86416212	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr12:86318600-86324600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links