Variant report

Variant	rs11011493
Chromosome Location	chr10:38493136-38493137
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs11011445	1.00[AMR][1000 genomes]
rs11011447	1.00[AMR][1000 genomes]
rs11011448	0.85[AMR][1000 genomes]
rs11011455	0.85[AMR][1000 genomes]
rs11011456	0.85[AMR][1000 genomes]
rs11011457	1.00[AMR][1000 genomes]
rs11011492	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11498331	1.00[EUR][1000 genomes]
rs12240841	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12243715	1.00[AMR][1000 genomes]
rs12244439	0.85[AMR][1000 genomes]
rs12244661	1.00[AMR][1000 genomes]
rs12245792	0.85[AMR][1000 genomes]
rs12246341	0.85[AMR][1000 genomes]
rs12246875	1.00[AMR][1000 genomes]
rs12247832	0.85[AMR][1000 genomes]
rs12248050	0.85[AMR][1000 genomes]
rs12248947	0.90[YRI][hapmap]
rs12252556	1.00[EUR][1000 genomes]
rs12254726	1.00[AMR][1000 genomes]
rs12257173	1.00[EUR][1000 genomes]
rs12257629	1.00[EUR][1000 genomes]
rs12258247	1.00[AMR][1000 genomes]
rs12260877	0.85[AMR][1000 genomes]
rs12261570	0.85[AMR][1000 genomes]
rs12261622	1.00[EUR][1000 genomes]
rs12266231	0.85[AMR][1000 genomes]
rs12266460	1.00[AMR][1000 genomes]
rs12268280	1.00[AMR][1000 genomes]
rs12775500	1.00[AMR][1000 genomes]
rs12782054	0.85[AMR][1000 genomes]
rs12784488	0.90[YRI][hapmap];1.00[AMR][1000 genomes]
rs16937701	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs28448364	1.00[AMR][1000 genomes]
rs28607758	1.00[AMR][1000 genomes]
rs28719516	1.00[AMR][1000 genomes]
rs34067956	0.85[AMR][1000 genomes]
rs34522767	0.85[AMR][1000 genomes]
rs34571803	1.00[AMR][1000 genomes]
rs34759610	0.85[AMR][1000 genomes]
rs34908048	1.00[AMR][1000 genomes]
rs35769459	1.00[EUR][1000 genomes]
rs36010363	0.85[AMR][1000 genomes]
rs36043070	0.85[AMR][1000 genomes]
rs36091737	0.85[AMR][1000 genomes]
rs36114117	1.00[AMR][1000 genomes]
rs58217854	0.85[AMR][1000 genomes]
rs59353999	1.00[EUR][1000 genomes]
rs7086341	0.90[YRI][hapmap]
rs7100316	0.83[EUR][1000 genomes]
rs71491237	1.00[AMR][1000 genomes]
rs71491239	0.85[AMR][1000 genomes]
rs71494838	1.00[EUR][1000 genomes]
rs71498883	1.00[EUR][1000 genomes]
rs7895219	0.85[AMR][1000 genomes]
rs7900878	1.00[AMR][1000 genomes]
rs7901183	0.90[YRI][hapmap];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	nsv540566	chr10:38301001-38680127	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv550419	chr10:38311777-38501654	Enhancers Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv895032	chr10:38427708-38498909	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv895033	chr10:38432348-38537070	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv947857	chr10:38453951-38497640	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island 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	chr10:38492600-38493600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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