Variant report

Variant	rs11237151
Chromosome Location	chr11:76960833-76960834
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:76960179..76961868-chr11:76980870..76982762,2	MCF-7	breast:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs11237141	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11237142	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11237148	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11237150	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11237160	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11237162	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11237164	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1125619	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11512967	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1225478	0.91[ASN][1000 genomes]
rs12361757	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12363707	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12363842	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12363944	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12366261	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12794253	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1377472	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1597954	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1622364	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1670446	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1670449	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1670450	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1670456	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1670458	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1670461	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1670462	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17824184	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1793468	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1793471	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1793472	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1793487	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1793490	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2156567	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2602476	0.87[ASN][1000 genomes]
rs2602483	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2602487	0.96[ASN][1000 genomes]
rs2725820	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2725822	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2725825	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2725828	0.96[ASN][1000 genomes]
rs34880271	0.91[ASN][1000 genomes]
rs4375461	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs472691	0.96[ASN][1000 genomes]
rs479104	0.87[ASN][1000 genomes]
rs493256	0.91[ASN][1000 genomes]
rs494289	0.91[ASN][1000 genomes]
rs508662	0.96[ASN][1000 genomes]
rs51500	0.91[ASN][1000 genomes]
rs522015	0.91[ASN][1000 genomes]
rs523481	0.96[ASN][1000 genomes]
rs535008	0.87[ASN][1000 genomes]
rs552323	0.91[ASN][1000 genomes]
rs557484	0.87[ASN][1000 genomes]
rs558470	0.96[ASN][1000 genomes]
rs560571	0.87[ASN][1000 genomes]
rs561386	0.96[ASN][1000 genomes]
rs562845	0.96[ASN][1000 genomes]
rs563731	0.87[ASN][1000 genomes]
rs572485	0.96[ASN][1000 genomes]
rs576220	0.96[ASN][1000 genomes]
rs580624	0.91[ASN][1000 genomes]
rs592602	0.96[ASN][1000 genomes]
rs598801	0.91[ASN][1000 genomes]
rs644551	0.96[ASN][1000 genomes]
rs649040	0.96[ASN][1000 genomes]
rs653792	0.91[ASN][1000 genomes]
rs66518011	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66540426	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66728428	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs674259	0.91[ASN][1000 genomes]
rs683455	0.87[ASN][1000 genomes]
rs683762	0.91[ASN][1000 genomes]
rs684793	0.87[ASN][1000 genomes]
rs686068	0.91[ASN][1000 genomes]
rs689108	0.87[ASN][1000 genomes]
rs7118943	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs883224	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs883680	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534515	chr11:76900813-77035769	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1048360	chr11:76900813-77387933	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv541089	chr11:76900813-77387933	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1049603	chr11:76900813-77520411	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv541090	chr11:76900813-77520411	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	esv2762917	chr11:76959189-76968918	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76956200-76963600	Weak transcription	Stomach Mucosa	stomach
2	chr11:76956400-76964800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:76956800-76961600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:76957000-76961800	Weak transcription	HepG2	liver
5	chr11:76957200-76970600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:76960200-76962200	Enhancers	NHEK	skin
7	chr11:76960200-76965000	Enhancers	HMEC	breast
8	chr11:76960400-76961600	Enhancers	HUVEC	blood vessel
9	chr11:76960400-76961800	Enhancers	NHDF-Ad	bronchial
10	chr11:76960400-76962400	Enhancers	NH-A	brain
11	chr11:76960400-76964000	Enhancers	Liver	Liver
12	chr11:76960400-76964600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:76960400-76965200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:76960600-76964600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:76960800-76961200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr11:76960800-76961800	Weak transcription	Osteobl	bone

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