Variant report

Variant	rs11226364
Chromosome Location	chr11:104315707-104315708
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10791696	0.80[AMR][1000 genomes]
rs10895665	0.80[AMR][1000 genomes]
rs10895667	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10895672	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10895673	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10895674	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10895675	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10895681	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10895690	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11226321	0.80[EUR][1000 genomes]
rs11226341	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11226343	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11226346	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11226348	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11226370	0.81[AMR][1000 genomes]
rs11600376	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11600631	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11602456	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11602492	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11602527	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11604356	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11604545	0.81[AMR][1000 genomes]
rs11605911	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11606581	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11608063	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12361853	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12362326	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12362336	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12362748	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12419882	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12787859	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12787993	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12791068	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12794711	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12795075	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12803570	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12807112	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12807863	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1487711	0.81[AMR][1000 genomes]
rs17102421	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17102463	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1825824	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1873095	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1873096	0.80[AMR][1000 genomes]
rs1873097	0.85[AMR][1000 genomes]
rs2220445	0.81[AMR][1000 genomes]
rs34076835	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34563542	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34623545	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34877813	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35273172	0.82[AMR][1000 genomes]
rs35859101	0.81[AMR][1000 genomes]
rs36056538	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4754111	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4754112	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4754114	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4755023	0.80[AMR][1000 genomes]
rs4755029	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4755034	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4755037	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4755038	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4755039	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7121183	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs71484353	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs71484355	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs71484360	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7951031	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs970530	0.81[AMR][1000 genomes]
rs970531	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760322	chr11:103760085-104374141	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1043976	chr11:103881236-104526403	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1040367	chr11:103956747-104440470	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1044271	chr11:104136156-104666252	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1046098	chr11:104207210-105003661	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv898350	chr11:104261833-104372318	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv898351	chr11:104274535-104368709	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv898352	chr11:104274535-104452042	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv898353	chr11:104274535-104497607	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv428579	chr11:104298339-104459797	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv826071	chr11:104306259-104368241	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv898354	chr11:104309414-104417374	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	esv3505102	chr11:104314842-104321840	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	esv3497011	chr11:104315142-104321890	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
15	nsv8867	chr11:104315561-104321194	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
16	esv3505101	chr11:104315683-104321136	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104314200-104316000	Enhancers	Fetal Heart	heart
2	chr11:104314600-104323200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:104315000-104316800	Enhancers	Stomach Mucosa	stomach
4	chr11:104315600-104315800	Enhancers	Fetal Lung	lung

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