Variant report

Variant	rs11011391
Chromosome Location	chr10:38163245-38163246
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10827821	0.82[AFR][1000 genomes]
rs10827830	0.94[AFR][1000 genomes]
rs10827834	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10827837	1.00[AMR][1000 genomes]
rs10827838	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11011332	0.82[AFR][1000 genomes]
rs11011356	0.94[AFR][1000 genomes]
rs11011357	0.94[AFR][1000 genomes]
rs11011358	0.88[AFR][1000 genomes]
rs11011368	0.94[AFR][1000 genomes]
rs11011375	0.94[AFR][1000 genomes]
rs11011385	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11011393	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11011403	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11011412	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11011415	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11011417	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11011428	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11011430	1.00[AMR][1000 genomes]
rs11011437	1.00[AMR][1000 genomes]
rs11812927	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11813723	1.00[AMR][1000 genomes]
rs11813932	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11814622	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11815775	0.82[AFR][1000 genomes]
rs11816307	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11816860	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11816995	0.94[AFR][1000 genomes]
rs11817782	0.82[AFR][1000 genomes]
rs11818933	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11819551	0.94[AFR][1000 genomes]
rs12241614	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12242131	0.82[AFR][1000 genomes]
rs12242343	1.00[AMR][1000 genomes]
rs12244864	0.82[AFR][1000 genomes]
rs12248857	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12250465	0.82[AFR][1000 genomes]
rs12251570	0.94[AFR][1000 genomes]
rs12252754	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12256181	0.94[AFR][1000 genomes]
rs12256794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12256916	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12257632	0.88[AFR][1000 genomes]
rs12257902	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12258024	0.94[AFR][1000 genomes]
rs12258128	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12260189	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12260310	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12262814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12266728	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12267847	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12268435	0.82[AFR][1000 genomes]
rs12269398	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12761218	0.82[AFR][1000 genomes]
rs12770231	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12773340	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12777107	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12779056	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12783599	0.82[AFR][1000 genomes]
rs34152840	0.82[AFR][1000 genomes]
rs34222428	0.94[AFR][1000 genomes]
rs34445730	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34591573	0.94[AFR][1000 genomes]
rs34964888	0.94[AFR][1000 genomes]
rs35047448	0.82[AFR][1000 genomes]
rs35056062	0.82[AFR][1000 genomes]
rs35404142	0.94[AFR][1000 genomes]
rs35818588	0.82[AFR][1000 genomes]
rs57753536	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60538050	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71489160	0.82[AFR][1000 genomes]
rs71491203	0.94[AFR][1000 genomes]
rs71491212	0.94[AFR][1000 genomes]
rs71491214	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71491223	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71491228	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71491229	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9651365	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1045684	chr10:37765361-38426204	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv540564	chr10:37765361-38426204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv1051121	chr10:38155991-38426204	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv540565	chr10:38155991-38426204	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 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	chr10:38155600-38176200	Weak transcription	Stomach Smooth Muscle	stomach

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