Variant report

Variant	rs56772860
Chromosome Location	chr6:24991172-24991173
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:24720596..24722709-chr6:24989331..24991417,2	K562	blood:
2	chr6:24858123..24860977-chr6:24989589..24991591,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000112308	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11964330	0.82[EUR][1000 genomes]
rs12110508	0.82[EUR][1000 genomes]
rs12111569	0.82[EUR][1000 genomes]
rs58272875	0.82[EUR][1000 genomes]
rs58446150	0.82[EUR][1000 genomes]
rs58858607	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59935869	1.00[EUR][1000 genomes]
rs60753079	1.00[EUR][1000 genomes]
rs73384104	1.00[EUR][1000 genomes]
rs73384120	0.90[EUR][1000 genomes]
rs73384131	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73384137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73384148	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73384155	0.82[EUR][1000 genomes]
rs73384157	0.82[EUR][1000 genomes]
rs73384158	0.82[EUR][1000 genomes]
rs73384159	0.82[EUR][1000 genomes]
rs73384162	0.82[EUR][1000 genomes]
rs73384168	0.82[EUR][1000 genomes]
rs73384170	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv1019504	chr6:24869174-24994758	Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv883482	chr6:24926730-25035920	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	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
6	nsv1030634	chr6:24938277-25040161	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	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

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24981200-24991800	Weak transcription	Thymus	Thymus
2	chr6:24981800-24992000	Weak transcription	Gastric	stomach
3	chr6:24982200-24991800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:24982400-24991800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:24984200-24995200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:24986000-24996600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:24986400-24992000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr6:24986400-24992800	Enhancers	Primary B cells from peripheral blood	blood
9	chr6:24986400-24995200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:24986400-24995400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr6:24986600-24992000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr6:24986600-24996600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:24987600-25000200	Weak transcription	Lung	lung
14	chr6:24988000-24991200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr6:24988200-24991800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr6:24988400-24992000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr6:24989000-24992000	Weak transcription	Dnd41	blood
18	chr6:24989200-24991200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr6:24989800-24991800	Enhancers	Primary B cells from cord blood	blood
20	chr6:24990000-24991800	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr6:24990000-24992800	Enhancers	Primary T cells fromperipheralblood	blood
22	chr6:24990200-24991200	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr6:24990200-24992200	Enhancers	Stomach Mucosa	stomach
24	chr6:24990400-24991600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:24990400-24991800	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr6:24990400-24991800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr6:24990400-24991800	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr6:24990400-24992600	Enhancers	Fetal Heart	heart
29	chr6:24990400-24992600	Enhancers	Hela-S3	cervix
30	chr6:24990400-24992600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr6:24990400-24992800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr6:24990400-24993800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr6:24990600-24991600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:24990600-24991600	Weak transcription	GM12878-XiMat	blood
35	chr6:24990600-24992200	Enhancers	HSMM	muscle
36	chr6:24990600-24992600	Enhancers	Primary hematopoietic stem cells	blood
37	chr6:24990600-24992600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr6:24990600-24992800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr6:24990600-24993000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr6:24990800-24991200	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr6:24990800-24991800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr6:24991000-24991400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr6:24991000-24991600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr6:24991000-24992000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr6:24991000-24992200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr6:24991000-24992400	Flanking Active TSS	Primary T cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links