Variant report

Variant	rs62565112
Chromosome Location	chr9:79092226-79092227
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:79091609..79094063-chr9:79133864..79136159,2	MCF-7	breast:
2	chr9:79086560..79088176-chr9:79091535..79093262,2	MCF-7	breast:
3	chr9:79072904..79074467-chr9:79090074..79092735,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000187210	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10119532	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11144922	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12237420	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3739516	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4526423	0.90[ASN][1000 genomes]
rs4745552	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62565119	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7019479	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7465809	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7858497	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs785934	0.83[ASN][1000 genomes]
rs785936	0.89[ASN][1000 genomes]
rs7862822	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7871849	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][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:50 , 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	chr9:79077600-79092800	Weak transcription	Fetal Stomach	stomach
4	chr9:79078600-79092400	Weak transcription	HMEC	breast
5	chr9:79080800-79117200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:79081800-79093000	Weak transcription	Lung	lung
7	chr9:79081800-79117200	Weak transcription	Gastric	stomach
8	chr9:79082600-79117600	Weak transcription	NHLF	lung
9	chr9:79083600-79092800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr9:79085200-79093000	Enhancers	Primary B cells from peripheral blood	blood
11	chr9:79086200-79093400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:79087400-79093000	Weak transcription	Fetal Thymus	thymus
13	chr9:79087600-79117400	Weak transcription	Colonic Mucosa	Colon
14	chr9:79087800-79093200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr9:79088200-79093200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr9:79088200-79093200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr9:79088400-79093000	Weak transcription	NHDF-Ad	bronchial
18	chr9:79088400-79093200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:79088400-79097000	Weak transcription	Stomach Mucosa	stomach
20	chr9:79088800-79092600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr9:79088800-79093000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr9:79088800-79093200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:79088800-79093200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr9:79088800-79093800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr9:79089000-79092400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr9:79089000-79093000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr9:79089000-79100800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:79089000-79103400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr9:79089000-79116400	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr9:79089800-79092600	Strong transcription	Fetal Intestine Small	intestine
31	chr9:79090000-79094000	Strong transcription	Osteobl	bone
32	chr9:79090400-79094200	Strong transcription	Muscle Satellite Cultured Cells	--
33	chr9:79090600-79094200	Strong transcription	Duodenum Mucosa	Duodenum
34	chr9:79091000-79092400	Weak transcription	HSMM	muscle
35	chr9:79091000-79092600	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr9:79091000-79093200	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr9:79091000-79093200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr9:79091200-79092600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr9:79091200-79092600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr9:79091200-79093000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr9:79091200-79093000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr9:79091200-79093200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr9:79091200-79108800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr9:79091400-79093000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr9:79091600-79092800	Weak transcription	Primary B cells from cord blood	blood
46	chr9:79091600-79093000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr9:79091800-79092600	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr9:79092000-79092600	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr9:79092200-79093800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr9:79092200-79093800	Strong transcription	Fetal Intestine Large	intestine

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