Variant report

Variant	rs28515035
Chromosome Location	chr6:2197318-2197319
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:2191098..2193029-chr6:2196230..2198209,2	MCF-7	breast:
2	chr6:1610715..1613985-chr6:2196585..2199138,3	MCF-7	breast:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1006019	0.83[AMR][1000 genomes]
rs17134714	0.83[AMR][1000 genomes]
rs2038223	0.83[AMR][1000 genomes]
rs2038224	0.83[AMR][1000 genomes]
rs55937718	0.83[AMR][1000 genomes]
rs56913552	0.83[AMR][1000 genomes]
rs58343222	0.83[AMR][1000 genomes]
rs59370688	0.83[AMR][1000 genomes]
rs60593022	0.83[AMR][1000 genomes]
rs60813424	0.83[AMR][1000 genomes]
rs61070654	0.83[AMR][1000 genomes]
rs6900870	0.83[AMR][1000 genomes]
rs6920255	0.83[AMR][1000 genomes]
rs6921705	0.83[AMR][1000 genomes]
rs73418780	0.83[AMR][1000 genomes]
rs73420706	0.83[AMR][1000 genomes]
rs73420724	0.83[AMR][1000 genomes]
rs9328083	0.83[AMR][1000 genomes]
rs9501809	0.83[AMR][1000 genomes]
rs9503104	0.83[AMR][1000 genomes]
rs9503108	0.83[AMR][1000 genomes]
rs9503112	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 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	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
10	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
11	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:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2185600-2197400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:2189200-2197600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:2189600-2202800	Weak transcription	Pancreas	Pancrea
4	chr6:2191000-2197600	Weak transcription	Left Ventricle	heart
5	chr6:2191200-2203400	Weak transcription	Primary T cells from cord blood	blood
6	chr6:2191800-2198000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:2192800-2222000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr6:2193200-2197600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:2193200-2197600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:2193800-2197600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:2193800-2206600	Weak transcription	Fetal Intestine Small	intestine
12	chr6:2193800-2216800	Weak transcription	Gastric	stomach
13	chr6:2194400-2198600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:2195200-2202800	Weak transcription	Aorta	Aorta
15	chr6:2196400-2197600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:2196400-2198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:2196400-2198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:2196400-2198000	Enhancers	Adipose Nuclei	Adipose
19	chr6:2196600-2197400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr6:2196600-2197400	Enhancers	Primary B cells from cord blood	blood
21	chr6:2196600-2197600	Enhancers	Primary B cells from peripheral blood	blood
22	chr6:2196600-2197800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr6:2196600-2197800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr6:2196600-2197800	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr6:2196600-2197800	Enhancers	Hela-S3	cervix
26	chr6:2196600-2198000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr6:2196600-2198000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:2196600-2198200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:2196600-2198400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr6:2196800-2197400	Weak transcription	HUVEC	blood vessel
31	chr6:2196800-2197600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr6:2196800-2197800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr6:2196800-2198000	Enhancers	NHLF	lung
34	chr6:2196800-2198600	Enhancers	Osteobl	bone
35	chr6:2197000-2198000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:2197000-2198200	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr6:2197000-2198200	Enhancers	HMEC	breast
38	chr6:2197000-2202600	Weak transcription	HepG2	liver
39	chr6:2197200-2197400	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr6:2197200-2197600	Weak transcription	Stomach Mucosa	stomach
41	chr6:2197200-2198000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr6:2197200-2198200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:2197200-2198400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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