Variant report

Variant	rs4269509
Chromosome Location	chr8:95898480-95898481
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr8:95895416-95899444	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:95890413..95893723-chr8:95897125..95900622,4	K562	blood:
2	chr8:95890906..95892878-chr8:95897475..95900324,2	MCF-7	breast:
3	chr8:95893455..95896139-chr8:95897032..95901216,5	MCF-7	breast:
4	chr8:95887273..95889571-chr8:95897523..95899180,2	K562	blood:

Variant related genes	Relation type
ENSG00000243979	TF binding region
ENSG00000164941	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs2305466	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28399556	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28399561	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57099803	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7844910	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv532338	chr8:95296118-95971825	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv891203	chr8:95883232-95948202	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh 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	19 gene(s)	inside rSNPs	diseases
5	nsv891204	chr8:95883232-95965135	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95837000-95905600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:95837400-95898800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr8:95838200-95905600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:95839400-95904400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr8:95870200-95905200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr8:95870600-95905600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr8:95873800-95898800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:95874200-95899000	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr8:95874400-95902600	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr8:95874400-95904600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr8:95875600-95904400	Strong transcription	Fetal Thymus	thymus
12	chr8:95876200-95899200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:95876200-95906600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr8:95876800-95899600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:95877000-95899200	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr8:95879200-95906600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr8:95881200-95905800	Weak transcription	Spleen	Spleen
18	chr8:95882200-95906600	Weak transcription	Gastric	stomach
19	chr8:95883400-95905600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:95883600-95905600	Weak transcription	Small Intestine	intestine
21	chr8:95883800-95899200	Strong transcription	NHDF-Ad	bronchial
22	chr8:95885000-95899400	Strong transcription	K562	blood
23	chr8:95885400-95898800	Strong transcription	Brain Inferior Temporal Lobe	brain
24	chr8:95886000-95905600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr8:95886000-95906400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:95886800-95899200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr8:95887200-95899200	Strong transcription	Osteobl	bone
28	chr8:95887200-95904600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr8:95887600-95906200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr8:95888200-95906600	Weak transcription	Ovary	ovary
31	chr8:95888600-95899200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr8:95889800-95898800	Strong transcription	Hela-S3	cervix
33	chr8:95890000-95906200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr8:95890200-95906600	Weak transcription	Lung	lung
35	chr8:95890600-95898600	Weak transcription	Pancreas	Pancrea
36	chr8:95890600-95906800	Weak transcription	Aorta	Aorta
37	chr8:95890800-95905800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr8:95890800-95905800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr8:95890800-95905800	Weak transcription	Psoas Muscle	Psoas
40	chr8:95891000-95906600	Weak transcription	Left Ventricle	heart
41	chr8:95891400-95905400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr8:95891400-95905600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr8:95891600-95904800	Weak transcription	Fetal Heart	heart
44	chr8:95891800-95905800	Weak transcription	Esophagus	oesophagus
45	chr8:95891800-95906000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr8:95892200-95898600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr8:95892400-95906400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr8:95893600-95905800	Weak transcription	HepG2	liver
49	chr8:95893800-95899400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:95893800-95906000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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