Variant report

Variant	rs2959768
Chromosome Location	chr8:6417375-6417376
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	chr8:6417306..6418909-chr8:6419114..6421148,2	K562	blood:

Variant related genes	Relation type
ENSG00000091879	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10103026	0.97[ASN][1000 genomes]
rs1562714	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1562715	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2167072	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2442509	1.00[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs2442591	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs2515505	1.00[GIH][hapmap];1.00[TSI][hapmap]
rs2515507	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2515508	1.00[CHB][hapmap];0.89[JPT][hapmap];0.95[ASN][1000 genomes]
rs2515509	1.00[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs2515513	0.81[ASN][1000 genomes]
rs28539969	0.97[ASN][1000 genomes]
rs2922808	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2922816	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2922864	0.87[ASN][1000 genomes]
rs2922884	0.97[ASN][1000 genomes]
rs2922890	0.97[ASN][1000 genomes]
rs2922893	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2922894	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2959763	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2959764	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2959765	0.97[ASN][1000 genomes]
rs2959767	0.95[ASN][1000 genomes]
rs2959769	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3020227	0.92[ASN][1000 genomes]
rs3020229	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3020230	0.97[ASN][1000 genomes]
rs3020231	0.97[ASN][1000 genomes]
rs3020232	0.97[ASN][1000 genomes]
rs3020233	1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3020234	0.97[ASN][1000 genomes]
rs3020235	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3020236	0.97[ASN][1000 genomes]
rs56954299	0.92[ASN][1000 genomes]
rs61131320	0.92[ASN][1000 genomes]
rs6991221	1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[ASN][1000 genomes]
rs7004238	1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs73507187	1.00[ASN][1000 genomes]
rs73507189	1.00[ASN][1000 genomes]
rs9314604	1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890034	chr8:5926632-6427868	Enhancers Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1021175	chr8:5965453-6880364	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv1027682	chr8:6018123-6920312	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	esv3506199	chr8:6116693-6536592	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
5	esv3506200	chr8:6116693-6536592	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
6	nsv933282	chr8:6261036-6440592	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1015981	chr8:6286575-6578450	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
8	nsv1027313	chr8:6286575-6920312	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
9	nsv890057	chr8:6317165-6427868	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1021684	chr8:6350091-6809455	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
11	esv2422383	chr8:6362389-6781593	Enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
12	nsv610004	chr8:6402366-6772913	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
13	nsv1029241	chr8:6411300-6761720	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6342400-6421400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr8:6364200-6478200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr8:6373600-6420200	Weak transcription	Esophagus	oesophagus
4	chr8:6386200-6417400	Weak transcription	Pancreas	Pancrea
5	chr8:6405800-6418400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr8:6405800-6419400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr8:6405800-6419400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr8:6406000-6417400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:6406000-6417400	Weak transcription	Aorta	Aorta
10	chr8:6407800-6423800	Weak transcription	Spleen	Spleen
11	chr8:6408800-6418400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr8:6408800-6419400	Weak transcription	Fetal Stomach	stomach
13	chr8:6410400-6419000	Weak transcription	Primary T cells from cord blood	blood
14	chr8:6411000-6419800	Weak transcription	Colonic Mucosa	Colon
15	chr8:6412400-6417400	Weak transcription	Fetal Intestine Large	intestine
16	chr8:6413600-6419400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr8:6414600-6417600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:6414600-6417600	Enhancers	Placenta Amnion	Placenta Amnion
19	chr8:6414600-6417600	Enhancers	NHEK	skin
20	chr8:6414800-6417600	Enhancers	HMEC	breast
21	chr8:6415000-6417400	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:6415200-6417400	Weak transcription	Left Ventricle	heart
23	chr8:6415200-6424000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:6415400-6418000	Enhancers	Primary hematopoietic stem cells	blood
25	chr8:6415400-6419000	Enhancers	NHLF	lung
26	chr8:6415400-6419400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr8:6415600-6420200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:6415800-6418000	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr8:6416000-6417400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:6416000-6417400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr8:6416000-6417600	Enhancers	HSMM	muscle
32	chr8:6416000-6417800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr8:6416000-6419600	Flanking Active TSS	HUVEC	blood vessel
34	chr8:6416200-6417400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr8:6416400-6418400	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr8:6416400-6418400	Enhancers	Fetal Thymus	thymus
37	chr8:6416400-6418800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr8:6416400-6419400	Enhancers	Primary B cells from cord blood	blood
39	chr8:6416400-6420800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:6416400-6422200	Enhancers	Primary B cells from peripheral blood	blood
41	chr8:6416600-6417400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr8:6416600-6417600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:6416600-6417600	Enhancers	Small Intestine	intestine
44	chr8:6416600-6417600	Flanking Active TSS	NH-A	brain
45	chr8:6416600-6417600	Flanking Active TSS	Osteobl	bone
46	chr8:6416600-6417800	Enhancers	HepG2	liver
47	chr8:6416600-6418400	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr8:6416600-6418800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:6416600-6418800	Enhancers	Fetal Intestine Small	intestine
50	chr8:6416600-6418800	Enhancers	Stomach Mucosa	stomach

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