Variant report

Variant	rs503406
Chromosome Location	chr11:77108136-77108137
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs11237200	0.82[JPT][hapmap]
rs11820118	0.83[JPT][hapmap]
rs11828786	0.83[JPT][hapmap]
rs1225478	0.85[EUR][1000 genomes]
rs1237490	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2154754	1.00[CHB][hapmap];0.88[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2602471	0.82[JPT][hapmap]
rs2602473	0.83[JPT][hapmap]
rs2602474	0.82[JPT][hapmap]
rs2602475	0.82[JPT][hapmap]
rs2602476	0.94[EUR][1000 genomes]
rs2602487	0.86[EUR][1000 genomes]
rs2725829	0.82[JPT][hapmap]
rs2729756	0.81[JPT][hapmap]
rs2844327	0.82[JPT][hapmap]
rs2852388	0.82[JPT][hapmap]
rs2852390	0.82[JPT][hapmap]
rs2853085	0.82[JPT][hapmap]
rs2853095	0.83[JPT][hapmap]
rs2888377	0.83[JPT][hapmap]
rs3015982	0.94[EUR][1000 genomes]
rs3015983	0.92[EUR][1000 genomes]
rs3015985	0.92[EUR][1000 genomes]
rs3015986	0.91[EUR][1000 genomes]
rs3015988	0.91[EUR][1000 genomes]
rs3015990	0.91[EUR][1000 genomes]
rs3015992	0.87[EUR][1000 genomes]
rs3019233	0.93[EUR][1000 genomes]
rs3019234	0.93[EUR][1000 genomes]
rs3019235	0.92[EUR][1000 genomes]
rs3019236	0.93[EUR][1000 genomes]
rs3019249	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3019257	0.92[EUR][1000 genomes]
rs34025917	0.87[EUR][1000 genomes]
rs34880271	0.92[EUR][1000 genomes]
rs472691	0.96[EUR][1000 genomes]
rs476258	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs479104	0.94[EUR][1000 genomes]
rs493256	0.96[EUR][1000 genomes]
rs494289	0.88[EUR][1000 genomes]
rs4945161	0.95[CHB][hapmap]
rs505841	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs508662	0.96[EUR][1000 genomes]
rs51500	0.93[EUR][1000 genomes]
rs520938	0.89[EUR][1000 genomes]
rs522015	0.94[EUR][1000 genomes]
rs523481	0.97[EUR][1000 genomes]
rs531638	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs535008	0.96[EUR][1000 genomes]
rs552323	0.97[EUR][1000 genomes]
rs557484	0.96[EUR][1000 genomes]
rs558470	0.96[EUR][1000 genomes]
rs560571	0.94[EUR][1000 genomes]
rs561386	0.97[EUR][1000 genomes]
rs562845	0.96[EUR][1000 genomes]
rs563731	0.96[EUR][1000 genomes]
rs572485	0.96[EUR][1000 genomes]
rs576220	0.95[EUR][1000 genomes]
rs580624	0.97[EUR][1000 genomes]
rs592602	0.88[EUR][1000 genomes]
rs595654	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs598801	0.92[EUR][1000 genomes]
rs644551	0.97[EUR][1000 genomes]
rs649040	0.97[EUR][1000 genomes]
rs653792	0.93[EUR][1000 genomes]
rs657269	0.81[EUR][1000 genomes]
rs674259	0.94[EUR][1000 genomes]
rs683455	0.95[EUR][1000 genomes]
rs683762	0.96[EUR][1000 genomes]
rs684793	0.95[EUR][1000 genomes]
rs686068	0.92[EUR][1000 genomes]
rs689108	0.94[EUR][1000 genomes]
rs7934230	0.91[EUR][1000 genomes]
rs7949721	0.89[EUR][1000 genomes]
rs876319	0.82[JPT][hapmap]
rs947810	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	esv3424135	chr11:76961603-77277087	Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1037724	chr11:77061945-77250391	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv541091	chr11:77061945-77250391	Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	esv3437433	chr11:77101280-77291686	Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77046800-77121600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:77055200-77117600	Weak transcription	Pancreas	Pancrea
3	chr11:77067200-77111800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr11:77084000-77111400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:77084600-77121200	Weak transcription	Thymus	Thymus
6	chr11:77086600-77120000	Weak transcription	Spleen	Spleen
7	chr11:77090800-77111200	Weak transcription	HMEC	breast
8	chr11:77091000-77108200	Weak transcription	Brain Angular Gyrus	brain
9	chr11:77091000-77112000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:77091000-77113400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr11:77091000-77117000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr11:77091000-77117600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:77093600-77117800	Weak transcription	NH-A	brain
14	chr11:77094000-77118400	Weak transcription	NHLF	lung
15	chr11:77094200-77111800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr11:77094200-77118200	Weak transcription	NHDF-Ad	bronchial
17	chr11:77094200-77118400	Weak transcription	Colonic Mucosa	Colon
18	chr11:77095400-77121000	Weak transcription	Fetal Thymus	thymus
19	chr11:77095800-77118600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr11:77097800-77111200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr11:77097800-77111200	Weak transcription	Fetal Muscle Leg	muscle
22	chr11:77098000-77121200	Weak transcription	Placenta	Placenta
23	chr11:77098200-77118400	Weak transcription	Fetal Stomach	stomach
24	chr11:77102600-77112400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr11:77102800-77111800	Weak transcription	Fetal Lung	lung
26	chr11:77102800-77116400	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr11:77103000-77118400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr11:77103000-77121400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr11:77103200-77108600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr11:77103200-77112800	Weak transcription	Primary B cells from cord blood	blood
31	chr11:77103600-77109600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr11:77103800-77121000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr11:77103800-77122000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:77104000-77112600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr11:77104200-77108400	Weak transcription	Primary T cells from cord blood	blood
36	chr11:77104200-77108600	Weak transcription	Fetal Kidney	kidney
37	chr11:77104200-77111800	Weak transcription	HSMM	muscle
38	chr11:77104600-77111800	Weak transcription	Colon Smooth Muscle	Colon
39	chr11:77104600-77118400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:77106000-77108800	Enhancers	Duodenum Mucosa	Duodenum
41	chr11:77106000-77109000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr11:77106000-77109000	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr11:77106000-77109000	Enhancers	Stomach Mucosa	stomach
44	chr11:77106000-77109800	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr11:77106400-77109200	Enhancers	Liver	Liver
46	chr11:77106600-77109000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr11:77106800-77108600	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr11:77106800-77108800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr11:77106800-77108800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr11:77106800-77108800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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