Variant report

Variant	rs11823120
Chromosome Location	chr11:105396613-105396614
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10160500	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10502048	0.85[ASN][1000 genomes]
rs10502055	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10895814	0.81[ASN][1000 genomes]
rs10895826	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1113611	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11226739	0.81[ASN][1000 genomes]
rs11226748	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11601207	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11601213	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11603521	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11603652	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11604474	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12270282	0.85[ASN][1000 genomes]
rs12271138	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12277692	0.85[ASN][1000 genomes]
rs12284832	0.96[ASN][1000 genomes]
rs12287628	0.87[ASN][1000 genomes]
rs12287683	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12288207	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17381570	0.80[EUR][1000 genomes]
rs17466579	0.80[EUR][1000 genomes]
rs17468921	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1945955	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1945956	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1945958	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1945963	0.95[ASN][1000 genomes]
rs1945977	0.81[ASN][1000 genomes]
rs2032412	0.83[ASN][1000 genomes]
rs2032413	0.83[ASN][1000 genomes]
rs4427540	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4619125	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55684902	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55716661	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55860203	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55885845	0.83[ASN][1000 genomes]
rs55888831	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55954762	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55957580	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56024169	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56219931	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56334909	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58893767	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60064890	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61891497	0.80[EUR][1000 genomes]
rs61891502	0.94[ASN][1000 genomes]
rs61891511	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61891543	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61891544	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61891545	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61891548	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61900581	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61900587	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61900598	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61900606	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61900607	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7120172	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7121772	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7122612	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7125326	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72981816	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72981829	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72986173	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7924758	0.81[ASN][1000 genomes]
rs7927980	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7934954	0.83[ASN][1000 genomes]
rs7935262	0.81[ASN][1000 genomes]
rs7938098	0.81[ASN][1000 genomes]
rs7943657	0.94[ASN][1000 genomes]
rs9651715	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9804516	0.85[ASN][1000 genomes]
rs9988916	0.81[ASN][1000 genomes]
rs9988917	0.80[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	nsv949337	chr11:104950007-105510193	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr11:105395000-105396800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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