Variant report

Variant	rs12280831
Chromosome Location	chr11:26002241-26002242
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:69)

rs_ID	r²[population]
rs1025835	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10501029	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10501031	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11029049	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11029053	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029054	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029055	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11029058	1.00[ASN][1000 genomes]
rs11029059	1.00[ASN][1000 genomes]
rs11029060	1.00[ASN][1000 genomes]
rs11029061	1.00[ASN][1000 genomes]
rs11029062	0.93[ASN][1000 genomes]
rs11029063	1.00[ASN][1000 genomes]
rs11029065	0.88[AMR][1000 genomes]
rs12270523	0.82[ASN][1000 genomes]
rs12271587	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12272161	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12273324	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12273504	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12273555	0.89[ASN][1000 genomes]
rs12273620	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12273640	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12273759	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12273808	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12274263	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12274928	1.00[EUR][1000 genomes]
rs12275369	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12275747	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12277460	1.00[ASN][1000 genomes]
rs12277478	1.00[ASN][1000 genomes]
rs12279309	1.00[ASN][1000 genomes]
rs12279540	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12280607	0.89[ASN][1000 genomes]
rs12281204	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12284543	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12286887	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12287905	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12288238	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs12288618	1.00[EUR][1000 genomes]
rs12288722	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12288725	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12289013	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12289848	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12290504	1.00[ASN][1000 genomes]
rs12292996	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12293071	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12293233	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12294235	1.00[ASN][1000 genomes]
rs1348165	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1352567	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1441492	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1441508	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1489515	1.00[ASN][1000 genomes]
rs1489516	1.00[ASN][1000 genomes]
rs1489517	1.00[ASN][1000 genomes]
rs16915021	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2008347	0.89[ASN][1000 genomes]
rs2012510	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56895836	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57197050	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57969155	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58165900	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs60147714	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs60412021	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7104747	0.96[ASN][1000 genomes]
rs7118878	0.96[ASN][1000 genomes]
rs984396	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs985289	1.00[ASN][1000 genomes]
rs985290	1.00[ASN][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	esv2760599	chr11:25186984-26159450	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046507	chr11:25469712-26111707	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv832091	chr11:25823826-26009887	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv469948	chr11:25859783-26026233	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1041778	chr11:25898574-26098141	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	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	chr11:26002000-26003200	Enhancers	Fetal Brain Male	brain

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