Variant report

Variant	rs4503499
Chromosome Location	chr11:101434168-101434169
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10791495	0.82[CHB][hapmap]
rs10791496	0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs10791497	0.88[ASN][1000 genomes]
rs10791498	0.88[ASN][1000 genomes]
rs10791499	0.88[ASN][1000 genomes]
rs10791500	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10791503	0.99[ASN][1000 genomes]
rs10791504	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10791505	0.86[EUR][1000 genomes]
rs10895135	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10895140	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10895141	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10895142	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10895143	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10895150	0.88[CEU][hapmap]
rs11224829	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.87[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11224839	0.89[ASN][1000 genomes]
rs11224846	0.92[ASN][1000 genomes]
rs11224852	0.95[CHB][hapmap];0.90[JPT][hapmap];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11224853	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11224855	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs11224864	0.86[EUR][1000 genomes]
rs11224877	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs11224880	0.82[CEU][hapmap]
rs12226165	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12419234	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12786241	0.89[ASN][1000 genomes]
rs12801488	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17096904	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17134809	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs36168048	0.83[EUR][1000 genomes]
rs3824934	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs4237603	0.83[CHB][hapmap];0.93[CHD][hapmap];0.86[JPT][hapmap]
rs4326755	0.83[CHB][hapmap]
rs4331057	0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs4331058	0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs4408275	0.83[CHB][hapmap]
rs4462305	0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs4469858	0.83[CHB][hapmap];0.91[CHD][hapmap];0.81[JPT][hapmap]
rs4480511	0.89[ASN][1000 genomes]
rs4486597	0.89[ASN][1000 genomes]
rs4492784	0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs4531428	0.83[CHB][hapmap];0.93[CHD][hapmap];0.81[JPT][hapmap]
rs4603270	0.86[ASN][1000 genomes]
rs4754012	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs4754013	0.88[ASN][1000 genomes]
rs4754014	0.89[ASN][1000 genomes]
rs4754770	0.89[ASN][1000 genomes]
rs4754771	0.89[ASN][1000 genomes]
rs4754774	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs4754776	0.87[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs4754777	0.83[CHB][hapmap];0.93[CHD][hapmap];0.86[JPT][hapmap]
rs4754779	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6590888	0.99[ASN][1000 genomes]
rs6590889	0.98[ASN][1000 genomes]
rs7109771	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7123327	0.99[ASN][1000 genomes]
rs7125565	0.86[ASN][1000 genomes]
rs7128797	0.88[ASN][1000 genomes]
rs7481496	0.86[EUR][1000 genomes]
rs7927579	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs7932338	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7936514	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs9326314	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs9888232	0.83[CHB][hapmap];0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv556131	chr11:100985777-101480017	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv530644	chr11:101010088-101486038	Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv898330	chr11:101243644-101722031	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv556134	chr11:101398450-101436689	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv556135	chr11:101399510-101436689	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv519281	chr11:101404645-101436689	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
7	nsv468852	chr11:101404645-101436689	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
8	nsv556136	chr11:101404645-101436689	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
9	nsv556137	chr11:101405218-101436689	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
10	esv2761703	chr11:101406049-101439667	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
11	nsv556138	chr11:101409478-101436997	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
12	esv2754308	chr11:101409790-101502790	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101416400-101437400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr11:101424400-101437200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr11:101426400-101447600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:101429600-101437400	Weak transcription	Ovary	ovary
5	chr11:101431400-101437400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr11:101433400-101434800	Enhancers	NHDF-Ad	bronchial
7	chr11:101433600-101434600	Enhancers	NHLF	lung
8	chr11:101434000-101434600	Enhancers	Sigmoid Colon	Sigmoid Colon

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