Variant report

Variant	rs11954634
Chromosome Location	chr5:114335047-114335048
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10039781	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10055823	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10061081	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10061288	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10077885	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10078015	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10477526	0.86[EUR][1000 genomes]
rs10478215	0.89[ASN][1000 genomes]
rs11241296	0.88[ASN][1000 genomes]
rs11241305	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13175861	0.87[ASN][1000 genomes]
rs1453011	0.93[ASN][1000 genomes]
rs1453025	0.81[ASN][1000 genomes]
rs28424064	0.89[ASN][1000 genomes]
rs3925317	0.83[ASN][1000 genomes]
rs4073838	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4073839	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4075509	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4075510	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4076057	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4131436	0.86[EUR][1000 genomes]
rs4131437	0.86[EUR][1000 genomes]
rs4235764	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4235765	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4235768	0.82[EUR][1000 genomes]
rs4235769	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4235770	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4286654	0.86[EUR][1000 genomes]
rs4312873	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4360034	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4382158	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4392610	0.81[EUR][1000 genomes]
rs4421095	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4485921	0.81[EUR][1000 genomes]
rs4485922	0.81[EUR][1000 genomes]
rs4489055	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4499823	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4554207	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4577683	0.84[ASN][1000 genomes]
rs4705696	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6869551	0.86[EUR][1000 genomes]
rs7701456	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7722841	0.82[EUR][1000 genomes]
rs7724117	0.80[ASN][1000 genomes]
rs995339	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882729	chr5:113743628-114497708	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1020798	chr5:113821828-114392727	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537867	chr5:113821828-114392727	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv830453	chr5:114277261-114546536	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv508376	chr5:114313533-114336531	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv4964	chr5:114318676-114359298	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3503914	chr5:114324253-114336151	Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
8	nsv1030649	chr5:114324590-114390181	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv3503915	chr5:114324603-114336001	Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
10	esv3503916	chr5:114325208-114335070	Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
11	esv3503917	chr5:114325208-114335070	Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
12	esv3470646	chr5:114325218-114335099	ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	n/a
13	esv3470645	chr5:114325273-114335058	Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a
14	esv3371408	chr5:114329053-114335051	Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114335000-114335200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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