Variant report

Variant	rs4682590
Chromosome Location	chr3:110212334-110212335
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs1022229	0.90[ASN][1000 genomes]
rs1028026	0.83[ASN][1000 genomes]
rs1028027	0.83[ASN][1000 genomes]
rs10511286	0.91[EUR][1000 genomes]
rs10934045	0.81[ASN][1000 genomes]
rs11713405	0.91[EUR][1000 genomes]
rs11715486	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11719761	0.84[EUR][1000 genomes]
rs11721302	0.91[EUR][1000 genomes]
rs12487462	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs12633463	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12633668	0.88[EUR][1000 genomes]
rs12637928	0.90[ASN][1000 genomes]
rs12638763	0.91[EUR][1000 genomes]
rs13058952	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13062461	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13065612	0.91[EUR][1000 genomes]
rs13069621	0.91[EUR][1000 genomes]
rs13070606	0.90[EUR][1000 genomes]
rs13078633	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[EUR][1000 genomes]
rs13081130	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13093393	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1398346	0.80[CHB][hapmap]
rs1398347	0.80[ASN][1000 genomes]
rs1398354	0.91[CHB][hapmap];0.86[JPT][hapmap]
rs1398410	0.87[ASN][1000 genomes]
rs1512540	0.81[ASN][1000 genomes]
rs1512660	0.81[ASN][1000 genomes]
rs1512661	0.81[ASN][1000 genomes]
rs1512681	0.93[ASN][1000 genomes]
rs1533208	0.81[ASN][1000 genomes]
rs1574700	0.81[ASN][1000 genomes]
rs17202417	0.84[EUR][1000 genomes]
rs17727387	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1849379	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1913088	0.81[ASN][1000 genomes]
rs2055966	0.91[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs2055967	0.80[ASN][1000 genomes]
rs2063567	0.92[ASN][1000 genomes]
rs2203187	0.90[ASN][1000 genomes]
rs2399335	0.91[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap]
rs34998073	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35156093	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35372780	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35859521	0.91[EUR][1000 genomes]
rs4682179	0.84[EUR][1000 genomes]
rs4682180	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4682181	0.80[ASN][1000 genomes]
rs4682182	0.96[CEU][hapmap];0.93[TSI][hapmap]
rs4682588	0.91[EUR][1000 genomes]
rs4682589	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4682594	0.81[ASN][1000 genomes]
rs4682596	0.96[CEU][hapmap];0.93[TSI][hapmap]
rs56067719	0.81[ASN][1000 genomes]
rs58500543	0.89[ASN][1000 genomes]
rs62271578	0.89[ASN][1000 genomes]
rs62271586	0.89[ASN][1000 genomes]
rs62271587	0.89[ASN][1000 genomes]
rs62271588	0.87[ASN][1000 genomes]
rs62271591	0.90[ASN][1000 genomes]
rs62271592	0.90[ASN][1000 genomes]
rs6437914	0.89[ASN][1000 genomes]
rs6771696	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6784648	0.80[ASN][1000 genomes]
rs6787448	0.91[EUR][1000 genomes]
rs6788158	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73217311	0.80[ASN][1000 genomes]
rs73217315	0.80[ASN][1000 genomes]
rs7613348	0.81[ASN][1000 genomes]
rs7626514	0.81[EUR][1000 genomes]
rs7628733	0.87[ASN][1000 genomes]
rs7630242	0.82[EUR][1000 genomes]
rs7638452	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7640587	0.81[ASN][1000 genomes]
rs7640755	0.91[CHB][hapmap];0.86[JPT][hapmap]
rs7640794	0.80[ASN][1000 genomes]
rs7644836	0.80[ASN][1000 genomes]
rs963346	0.90[ASN][1000 genomes]
rs9813893	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs9815868	0.91[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap]
rs9818091	0.90[ASN][1000 genomes]
rs9826577	0.81[ASN][1000 genomes]
rs9831873	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9843950	0.91[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap]
rs9846566	0.81[ASN][1000 genomes]
rs9851821	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9860708	0.81[ASN][1000 genomes]
rs9862336	0.92[ASN][1000 genomes]
rs9867550	0.81[ASN][1000 genomes]
rs9870835	0.90[ASN][1000 genomes]
rs9872133	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9877235	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9877472	0.81[ASN][1000 genomes]
rs9877920	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999414	chr3:110103126-110340180	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv829670	chr3:110134650-110308256	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv520365	chr3:110155172-110441165	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1001144	chr3:110158316-110431113	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv536687	chr3:110158316-110431113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1001810	chr3:110158316-110522247	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1010230	chr3:110204439-110588814	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv536688	chr3:110204439-110588814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv829672	chr3:110206693-110361632	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1011034	chr3:110209344-110559021	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv536689	chr3:110209344-110559021	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr3:110211600-110213400	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr3:110211600-110213400	Enhancers	Fetal Lung	lung

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