Variant report

Variant	rs7118878
Chromosome Location	chr11:26017508-26017509
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1025835	0.85[ASN][1000 genomes]
rs10501031	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11029049	0.85[ASN][1000 genomes]
rs11029053	0.96[ASN][1000 genomes]
rs11029054	0.96[ASN][1000 genomes]
rs11029055	0.96[ASN][1000 genomes]
rs11029058	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11029059	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11029060	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11029061	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11029062	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11029063	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11029065	0.81[AFR][1000 genomes]
rs12271587	0.96[ASN][1000 genomes]
rs12272161	0.96[ASN][1000 genomes]
rs12273324	0.96[ASN][1000 genomes]
rs12273504	0.96[ASN][1000 genomes]
rs12273555	0.85[ASN][1000 genomes]
rs12273620	0.96[ASN][1000 genomes]
rs12273640	0.96[ASN][1000 genomes]
rs12273759	0.96[ASN][1000 genomes]
rs12273808	0.96[ASN][1000 genomes]
rs12274263	0.96[ASN][1000 genomes]
rs12275747	0.96[ASN][1000 genomes]
rs12277460	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12277478	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12279309	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12279540	0.96[ASN][1000 genomes]
rs12280607	0.85[ASN][1000 genomes]
rs12280831	0.96[ASN][1000 genomes]
rs12281204	0.96[ASN][1000 genomes]
rs12284543	0.96[ASN][1000 genomes]
rs12286887	0.96[ASN][1000 genomes]
rs12287905	0.85[ASN][1000 genomes]
rs12288722	0.90[AFR][1000 genomes]
rs12288725	0.84[AFR][1000 genomes]
rs12289013	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12290504	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12294235	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1352567	0.96[ASN][1000 genomes]
rs1441508	0.85[ASN][1000 genomes]
rs1489515	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1489516	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1489517	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16915021	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2008347	0.85[ASN][1000 genomes]
rs2012510	0.96[ASN][1000 genomes]
rs4086865	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4086867	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56374149	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56895836	0.96[ASN][1000 genomes]
rs57197050	0.96[ASN][1000 genomes]
rs57969155	0.96[ASN][1000 genomes]
rs60412021	0.96[ASN][1000 genomes]
rs7104747	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs984396	0.96[ASN][1000 genomes]
rs985289	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs985290	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	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
4	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26017000-26017800	Enhancers	Fetal Heart	heart
2	chr11:26017400-26017800	Enhancers	Fetal Lung	lung

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