Variant report

Variant	rs9328083
Chromosome Location	chr6:2157887-2157888
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1006019	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1033533	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs13206375	0.90[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs13437488	0.90[YRI][hapmap]
rs163071	0.82[YRI][hapmap]
rs163072	0.82[YRI][hapmap]
rs17134714	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2038223	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2038224	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs234917	0.89[YRI][hapmap]
rs234918	0.90[YRI][hapmap]
rs234929	0.90[YRI][hapmap]
rs234945	0.82[YRI][hapmap]
rs234949	0.82[YRI][hapmap]
rs2483054	0.83[AMR][1000 genomes]
rs28515035	0.83[AMR][1000 genomes]
rs3800165	0.90[YRI][hapmap]
rs4959635	0.86[YRI][hapmap]
rs4959637	0.90[YRI][hapmap]
rs4959642	0.90[YRI][hapmap]
rs55847540	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs55937718	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56913552	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58343222	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58405376	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs59370688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59520004	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs60593022	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60813424	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61070654	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61096641	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs628510	0.83[AMR][1000 genomes]
rs6596871	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6900870	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6904830	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6909588	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6920255	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6921705	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6934917	0.90[YRI][hapmap]
rs73418780	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73420706	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73420724	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7757356	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9328084	0.90[YRI][hapmap]
rs9501806	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9501807	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9501808	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9501809	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9503101	0.97[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9503102	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9503103	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9503104	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9503108	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9503109	0.89[YRI][hapmap]
rs9503112	0.83[AMR][1000 genomes]
rs9503118	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs9503120	0.90[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530548	chr6:1441421-2351608	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv931941	chr6:1768439-2246781	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
4	nsv522608	chr6:2032259-2203888	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1025814	chr6:2064629-2308518	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
6	nsv538098	chr6:2064629-2308518	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
7	nsv1030181	chr6:2071210-2308657	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS 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	46 gene(s)	inside rSNPs	diseases
8	nsv538099	chr6:2071210-2308657	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
9	nsv883387	chr6:2086679-2176239	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv883388	chr6:2093432-2514911	Strong transcription Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
11	nsv883389	chr6:2093432-2776303	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
12	nsv830573	chr6:2120985-2263646	Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2128000-2160800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:2142600-2161000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr6:2143600-2161600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr6:2143600-2161600	Weak transcription	HepG2	liver
5	chr6:2149200-2159000	Weak transcription	Gastric	stomach
6	chr6:2156000-2158400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:2156000-2161800	Weak transcription	Small Intestine	intestine
8	chr6:2156800-2158000	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr6:2156800-2158200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:2157000-2159000	Enhancers	Muscle Satellite Cultured Cells	--
11	chr6:2157200-2158000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr6:2157200-2158200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:2157200-2158200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:2157200-2158400	Enhancers	HSMM	muscle
15	chr6:2157200-2158600	Enhancers	Adipose Nuclei	Adipose
16	chr6:2157200-2158600	Enhancers	NHLF	lung
17	chr6:2157200-2159200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr6:2157200-2159200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:2157200-2159200	Enhancers	HMEC	breast
20	chr6:2157200-2159200	Enhancers	NHDF-Ad	bronchial
21	chr6:2157400-2158000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr6:2157400-2158000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:2157400-2158000	Enhancers	NH-A	brain
24	chr6:2157400-2158000	Flanking Active TSS	Osteobl	bone
25	chr6:2157400-2158200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr6:2157400-2158200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr6:2157400-2158200	Enhancers	HSMMtube	muscle
28	chr6:2157400-2158400	Enhancers	NHEK	skin
29	chr6:2157400-2158800	Enhancers	Primary T cells from cord blood	blood
30	chr6:2157400-2159000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr6:2157400-2159000	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr6:2157400-2159200	Enhancers	Hela-S3	cervix
33	chr6:2157400-2159600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:2157600-2158000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr6:2157600-2158000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:2157600-2158000	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr6:2157600-2158000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr6:2157600-2158200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
39	chr6:2157600-2158200	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr6:2157600-2158400	Flanking Active TSS	GM12878-XiMat	blood
41	chr6:2157600-2158400	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr6:2157600-2159000	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr6:2157600-2159200	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr6:2157600-2159200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr6:2157600-2159200	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr6:2157600-2159200	Enhancers	Dnd41	blood
47	chr6:2157600-2164400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr6:2157800-2158400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:2157800-2159000	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr6:2157800-2159400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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