Variant report

Variant	rs9467388
Chromosome Location	chr6:25087952-25087953
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1002539	0.95[YRI][hapmap]
rs1037168	0.95[YRI][hapmap]
rs1046141	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs1046142	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs1128826	0.87[AFR][1000 genomes]
rs1128827	0.88[AFR][1000 genomes]
rs12332924	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12333217	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs12333219	0.88[AFR][1000 genomes]
rs12333222	0.88[AFR][1000 genomes]
rs12333327	0.87[AFR][1000 genomes]
rs1447242	0.95[YRI][hapmap]
rs16890067	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs16890087	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs16890100	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs2516576	0.94[YRI][hapmap];0.89[AFR][1000 genomes]
rs2516578	0.94[AFR][1000 genomes]
rs302983	0.90[YRI][hapmap]
rs3792978	0.94[YRI][hapmap]
rs3812107	0.94[YRI][hapmap]
rs3828730	0.94[YRI][hapmap]
rs3828731	0.95[YRI][hapmap]
rs4538700	1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs4711076	0.83[YRI][hapmap]
rs4712884	0.90[YRI][hapmap]
rs6456647	1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6456648	1.00[YRI][hapmap]
rs6905460	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs6905554	0.95[YRI][hapmap];0.89[AFR][1000 genomes]
rs6905624	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs6906421	0.89[AFR][1000 genomes]
rs6913324	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs6913346	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs6915329	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs6925889	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs6926671	0.97[AFR][1000 genomes]
rs6928763	0.94[YRI][hapmap]
rs7740848	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs7745550	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs7745609	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs7755584	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs7756507	0.85[AFR][1000 genomes]
rs7762804	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs7773107	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs7774557	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs916537	0.95[YRI][hapmap];0.89[AFR][1000 genomes]
rs916538	0.95[YRI][hapmap];0.89[AFR][1000 genomes]
rs916539	0.95[YRI][hapmap];0.89[AFR][1000 genomes]
rs9461096	0.85[YRI][hapmap]
rs9461098	0.95[YRI][hapmap]
rs9461101	0.88[AFR][1000 genomes]
rs9461104	0.95[YRI][hapmap];0.89[AFR][1000 genomes]
rs9461106	0.86[AFR][1000 genomes]
rs9467394	0.88[AFR][1000 genomes]
rs9467395	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs9467396	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs9467398	0.88[AFR][1000 genomes]
rs9467400	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs9467401	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs9467403	0.87[AFR][1000 genomes]
rs9467404	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs9467405	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs9467406	0.87[AFR][1000 genomes]
rs9467407	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9467408	0.87[AFR][1000 genomes]
rs9467409	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs9467410	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs9467411	0.95[YRI][hapmap];0.89[AFR][1000 genomes]

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	nsv1022966	chr6:24763776-25154212	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv538160	chr6:24763776-25154212	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1023989	chr6:24930362-25285679	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv830610	chr6:24951741-25124239	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	nsv830611	chr6:25039374-25199112	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	nsv470806	chr6:25082262-25156197	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv462662	chr6:25084718-25165486	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv601166	chr6:25084718-25165486	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25079400-25093000	Weak transcription	Ovary	ovary
2	chr6:25080400-25098000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:25081200-25092000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr6:25081600-25088800	Weak transcription	Osteobl	bone
5	chr6:25082200-25094800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr6:25082600-25105200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:25083800-25089800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:25083800-25093200	Weak transcription	Colonic Mucosa	Colon
9	chr6:25084200-25089800	Weak transcription	Hela-S3	cervix
10	chr6:25084800-25088400	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr6:25084800-25099000	Weak transcription	Fetal Intestine Large	intestine
12	chr6:25084800-25113800	Weak transcription	Gastric	stomach
13	chr6:25085000-25088600	Weak transcription	Lung	lung
14	chr6:25085000-25088600	Enhancers	HUVEC	blood vessel
15	chr6:25085200-25088000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr6:25085200-25089400	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr6:25085200-25108000	Weak transcription	Colon Smooth Muscle	Colon
18	chr6:25085400-25088200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:25085400-25091600	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr6:25085600-25088000	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr6:25085800-25088400	Genic enhancers	Dnd41	blood
22	chr6:25086200-25088600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:25086200-25096400	Strong transcription	Thymus	Thymus
24	chr6:25086400-25089800	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr6:25086400-25099600	Strong transcription	Placenta	Placenta
26	chr6:25086600-25090000	Strong transcription	Stomach Smooth Muscle	stomach
27	chr6:25086600-25090400	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr6:25086600-25096600	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr6:25086800-25088200	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr6:25086800-25088800	Enhancers	Primary T cells from cord blood	blood
31	chr6:25086800-25088800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:25087000-25089000	Weak transcription	Liver	Liver
33	chr6:25087000-25090600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr6:25087000-25093000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:25087000-25105400	Weak transcription	GM12878-XiMat	blood
36	chr6:25087200-25089000	Weak transcription	Spleen	Spleen
37	chr6:25087200-25090200	Genic enhancers	Primary hematopoietic stem cells	blood
38	chr6:25087200-25091400	Weak transcription	Esophagus	oesophagus
39	chr6:25087400-25088400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:25087400-25088400	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr6:25087400-25088600	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr6:25087400-25088800	Weak transcription	Adipose Nuclei	Adipose
43	chr6:25087400-25088800	Weak transcription	Aorta	Aorta
44	chr6:25087400-25089400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr6:25087400-25089600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:25087400-25089600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:25087400-25089800	Weak transcription	Left Ventricle	heart
48	chr6:25087400-25092200	Weak transcription	Primary B cells from cord blood	blood
49	chr6:25087400-25098200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr6:25087400-25101600	Weak transcription	Placenta Amnion	Placenta Amnion

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