Variant report

Variant	rs62565117
Chromosome Location	chr9:79095270-79095271
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11144922	0.83[EUR][1000 genomes]
rs4745552	0.82[EUR][1000 genomes]
rs62565119	0.80[EUR][1000 genomes]
rs7019479	0.82[EUR][1000 genomes]
rs7465809	0.82[EUR][1000 genomes]
rs7862822	0.82[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	nsv869152	chr9:78742197-79583399	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv931033	chr9:78850330-79366454	Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv893478	chr9:78933874-79101006	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv893479	chr9:78971253-79275226	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv949417	chr9:79078703-79282589	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:79075400-79101000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr9:79075600-79117800	Weak transcription	Primary T cells from cord blood	blood
3	chr9:79080800-79117200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:79081800-79117200	Weak transcription	Gastric	stomach
5	chr9:79082600-79117600	Weak transcription	NHLF	lung
6	chr9:79087600-79117400	Weak transcription	Colonic Mucosa	Colon
7	chr9:79088400-79097000	Weak transcription	Stomach Mucosa	stomach
8	chr9:79089000-79100800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr9:79089000-79103400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr9:79089000-79116400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:79091200-79108800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr9:79093400-79095400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:79093400-79101200	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr9:79093400-79102800	Weak transcription	Lung	lung
15	chr9:79093400-79142800	Weak transcription	Fetal Stomach	stomach
16	chr9:79093600-79095400	Weak transcription	Fetal Intestine Small	intestine
17	chr9:79093600-79100800	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr9:79093600-79103600	Weak transcription	Fetal Thymus	thymus
19	chr9:79093600-79111400	Weak transcription	NHDF-Ad	bronchial
20	chr9:79093600-79117200	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr9:79093800-79096800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr9:79093800-79098600	Weak transcription	Fetal Intestine Large	intestine
23	chr9:79093800-79098600	Weak transcription	HSMM	muscle
24	chr9:79093800-79101400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr9:79093800-79101400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr9:79093800-79101600	Weak transcription	Primary B cells from peripheral blood	blood
27	chr9:79093800-79101600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr9:79093800-79102000	Weak transcription	Primary B cells from cord blood	blood
29	chr9:79093800-79102200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr9:79093800-79103000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr9:79093800-79105400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr9:79093800-79109000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr9:79093800-79116600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:79093800-79117000	Weak transcription	HMEC	breast
35	chr9:79093800-79118000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr9:79094000-79100800	Weak transcription	Osteobl	bone
37	chr9:79094200-79096600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:79094200-79096600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr9:79094200-79101000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr9:79094200-79102000	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr9:79094200-79120200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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