Variant report

Variant	rs11224852
Chromosome Location	chr11:101425380-101425381
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10791495	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs10791496	0.91[CHB][hapmap];0.86[ASN][1000 genomes]
rs10791497	0.86[ASN][1000 genomes]
rs10791498	0.86[ASN][1000 genomes]
rs10791499	0.86[ASN][1000 genomes]
rs10791500	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10791503	0.86[ASN][1000 genomes]
rs10791504	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs10791505	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10895135	0.95[CHB][hapmap];0.91[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10895140	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs10895141	0.96[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs10895142	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10895143	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10895149	0.82[AMR][1000 genomes]
rs10895150	1.00[YRI][hapmap];0.82[AMR][1000 genomes]
rs11224829	0.95[CHB][hapmap];0.95[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11224839	0.87[ASN][1000 genomes]
rs11224846	0.91[ASN][1000 genomes]
rs11224853	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11224855	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs11224864	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11224877	0.86[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11224887	0.80[AMR][1000 genomes]
rs12226165	0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12419234	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12575190	0.80[AMR][1000 genomes]
rs12786241	0.87[ASN][1000 genomes]
rs12792618	0.80[AMR][1000 genomes]
rs12801488	0.96[CHB][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs17096904	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17134809	0.87[CHB][hapmap]
rs1938829	0.84[AMR][1000 genomes]
rs36168048	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3824934	1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4237603	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs4326755	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs4331057	0.87[CHB][hapmap];0.85[ASN][1000 genomes]
rs4331058	0.91[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs4408275	0.87[CHB][hapmap];0.95[JPT][hapmap]
rs4462305	0.87[CHB][hapmap];0.85[ASN][1000 genomes]
rs4469858	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs4480511	0.87[ASN][1000 genomes]
rs4486597	0.87[ASN][1000 genomes]
rs4492784	0.91[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs4503499	0.95[CHB][hapmap];0.90[JPT][hapmap];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4531428	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs4603270	0.85[ASN][1000 genomes]
rs4754012	0.87[CHB][hapmap]
rs4754013	0.86[ASN][1000 genomes]
rs4754014	0.87[ASN][1000 genomes]
rs4754770	0.87[ASN][1000 genomes]
rs4754771	0.87[ASN][1000 genomes]
rs4754774	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs4754776	0.91[CHB][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs4754777	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs4754779	0.96[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs6590888	0.86[ASN][1000 genomes]
rs6590889	0.85[ASN][1000 genomes]
rs7109771	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7123327	0.87[ASN][1000 genomes]
rs7125565	0.85[ASN][1000 genomes]
rs7128797	0.86[ASN][1000 genomes]
rs7481496	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7927579	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs7932338	0.95[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs7936514	0.91[CHB][hapmap];0.86[JPT][hapmap]
rs9326314	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs947991	0.80[AMR][1000 genomes]
rs9888232	0.87[CHB][hapmap];0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 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	nsv556133	chr11:101398450-101433161	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv556134	chr11:101398450-101436689	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv556135	chr11:101399510-101436689	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv519281	chr11:101404645-101436689	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
8	nsv468852	chr11:101404645-101436689	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
9	nsv556136	chr11:101404645-101436689	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
10	nsv556137	chr11:101405218-101436689	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
11	esv2761703	chr11:101406049-101439667	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
12	nsv556138	chr11:101409478-101436997	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
13	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:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101401200-101425800	Weak transcription	Ovary	ovary
2	chr11:101416400-101437400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:101422400-101427400	Enhancers	NHLF	lung
4	chr11:101423400-101425400	Enhancers	Primary B cells from cord blood	blood
5	chr11:101423600-101426400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:101423600-101426800	Enhancers	NHDF-Ad	bronchial
7	chr11:101423800-101425800	Enhancers	Primary B cells from peripheral blood	blood
8	chr11:101424200-101425800	Enhancers	Fetal Heart	heart
9	chr11:101424400-101437200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr11:101424600-101425800	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr11:101424800-101425400	Enhancers	GM12878-XiMat	blood
12	chr11:101424800-101426200	Enhancers	Colon Smooth Muscle	Colon

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