Variant report

Variant	rs4761985
Chromosome Location	chr12:51676473-51676474
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1362963	0.82[AFR][1000 genomes]
rs1991433	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2114876	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2288367	0.88[EUR][1000 genomes]
rs2359450	0.86[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs3210837	0.82[AFR][1000 genomes]
rs3858637	0.82[EUR][1000 genomes]
rs3969069	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4477479	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4611251	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4761982	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4761994	0.95[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs4762011	0.82[AFR][1000 genomes]
rs6580821	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7133314	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7135343	0.82[AFR][1000 genomes]
rs7135736	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7135840	0.82[AFR][1000 genomes]
rs7306505	0.82[AFR][1000 genomes]
rs7306875	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs7308177	0.81[EUR][1000 genomes]
rs7316221	0.81[EUR][1000 genomes]
rs7316604	0.81[EUR][1000 genomes]
rs74093810	0.81[EUR][1000 genomes]
rs74093814	0.81[EUR][1000 genomes]
rs7954976	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7957868	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7975715	0.81[EUR][1000 genomes]
rs9795976	0.88[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482304	chr12:51653496-51814917	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51664600-51683200	Weak transcription	Spleen	Spleen
2	chr12:51664600-51692800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:51664800-51685800	Weak transcription	Esophagus	oesophagus
4	chr12:51665400-51679800	Weak transcription	Liver	Liver
5	chr12:51665600-51678200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr12:51669400-51678200	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr12:51673200-51685200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr12:51673400-51684800	Weak transcription	GM12878-XiMat	blood
9	chr12:51673800-51679400	Strong transcription	Thymus	Thymus
10	chr12:51673800-51685400	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr12:51673800-51697600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr12:51674000-51680600	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr12:51674000-51683400	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr12:51674000-51698400	Strong transcription	Fetal Thymus	thymus
15	chr12:51674000-51701400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr12:51674200-51685400	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr12:51674200-51685600	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr12:51674200-51704000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr12:51674400-51679000	Strong transcription	Primary B cells from peripheral blood	blood
20	chr12:51674400-51685200	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr12:51674400-51698400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr12:51674400-51698600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:51674400-51698800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:51674400-51700600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr12:51674600-51685800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr12:51674600-51686000	Strong transcription	Primary T cells from cord blood	blood
27	chr12:51674800-51680000	Strong transcription	Primary B cells from cord blood	blood
28	chr12:51675000-51676800	Enhancers	Placenta	Placenta
29	chr12:51675000-51679400	Strong transcription	Primary T killer memory cells from peripheral blood	blood
30	chr12:51675200-51685600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr12:51675800-51676600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr12:51675800-51678000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr12:51675800-51678400	Weak transcription	HMEC	breast
34	chr12:51675800-51678600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:51675800-51679600	Weak transcription	Hela-S3	cervix
36	chr12:51675800-51681800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr12:51676000-51678000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr12:51676000-51678000	Weak transcription	NHEK	skin
39	chr12:51676000-51678200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:51676000-51680000	Strong transcription	Primary hematopoietic stem cells	blood
41	chr12:51676200-51678000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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