Variant report

Variant	rs7032475
Chromosome Location	chr9:79093167-79093168
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10114296	1.00[AMR][1000 genomes]
rs10116826	1.00[EUR][1000 genomes]
rs10116860	1.00[AMR][1000 genomes]
rs10117138	1.00[EUR][1000 genomes]
rs10119188	1.00[EUR][1000 genomes]
rs10120866	1.00[EUR][1000 genomes]
rs10120887	1.00[EUR][1000 genomes]
rs10124464	1.00[AMR][1000 genomes]
rs10125804	1.00[AMR][1000 genomes]
rs11144872	1.00[AMR][1000 genomes]
rs11144874	1.00[AMR][1000 genomes]
rs11144885	1.00[AMR][1000 genomes]
rs11144886	1.00[AMR][1000 genomes]
rs11144936	1.00[EUR][1000 genomes]
rs12000283	1.00[AMR][1000 genomes]
rs12000462	1.00[EUR][1000 genomes]
rs12003549	1.00[EUR][1000 genomes]
rs12003653	1.00[AMR][1000 genomes]
rs12338735	1.00[AMR][1000 genomes]
rs12340744	1.00[EUR][1000 genomes]
rs12343728	1.00[EUR][1000 genomes]
rs12345290	1.00[AMR][1000 genomes]
rs12346177	1.00[AMR][1000 genomes]
rs12346217	1.00[AMR][1000 genomes]
rs12346978	1.00[AMR][1000 genomes]
rs12349066	1.00[EUR][1000 genomes]
rs12349438	1.00[AMR][1000 genomes]
rs12352019	1.00[EUR][1000 genomes]
rs17062615	1.00[EUR][1000 genomes]
rs17062617	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17062620	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28391132	1.00[AMR][1000 genomes]
rs28435584	1.00[AMR][1000 genomes]
rs28477196	1.00[AMR][1000 genomes]
rs28591137	1.00[AMR][1000 genomes]
rs28607333	1.00[EUR][1000 genomes]
rs28704710	1.00[AMR][1000 genomes]
rs28803171	1.00[EUR][1000 genomes]
rs28837371	1.00[AMR][1000 genomes]
rs35340990	1.00[EUR][1000 genomes]
rs4606124	1.00[EUR][1000 genomes]
rs55841807	1.00[AMR][1000 genomes]
rs55843495	1.00[AMR][1000 genomes]
rs55868826	1.00[AMR][1000 genomes]
rs56914572	1.00[EUR][1000 genomes]
rs57011789	1.00[EUR][1000 genomes]
rs57699869	1.00[AMR][1000 genomes]
rs61328249	1.00[AMR][1000 genomes]
rs7018821	1.00[AMR][1000 genomes]
rs7022424	1.00[AMR][1000 genomes]
rs7022806	1.00[AMR][1000 genomes]
rs7022930	1.00[AMR][1000 genomes]
rs7026641	1.00[AMR][1000 genomes]
rs7027657	1.00[EUR][1000 genomes]
rs7030639	1.00[AMR][1000 genomes]
rs7031173	1.00[AMR][1000 genomes]
rs7039907	1.00[AMR][1000 genomes]
rs7042938	1.00[AMR][1000 genomes]
rs7045064	1.00[AMR][1000 genomes]
rs73464506	1.00[EUR][1000 genomes]
rs73650203	1.00[AMR][1000 genomes]
rs73650204	1.00[AMR][1000 genomes]
rs73650205	1.00[AMR][1000 genomes]
rs73650206	1.00[AMR][1000 genomes]
rs73650208	1.00[AMR][1000 genomes]
rs73650209	1.00[AMR][1000 genomes]
rs73650210	1.00[AMR][1000 genomes]
rs73650211	1.00[AMR][1000 genomes]
rs73650212	1.00[AMR][1000 genomes]
rs73650217	1.00[AMR][1000 genomes]
rs73650218	1.00[AMR][1000 genomes]
rs73650220	1.00[AMR][1000 genomes]
rs73652926	1.00[AMR][1000 genomes]
rs73652927	1.00[AMR][1000 genomes]
rs73652930	1.00[AMR][1000 genomes]
rs73652940	1.00[AMR][1000 genomes]
rs73652941	1.00[AMR][1000 genomes]
rs73652942	1.00[AMR][1000 genomes]
rs73652943	1.00[AMR][1000 genomes]
rs73652944	1.00[AMR][1000 genomes]
rs73652945	1.00[AMR][1000 genomes]
rs7863426	1.00[AMR][1000 genomes]
rs7867442	1.00[AMR][1000 genomes]
rs7874984	1.00[EUR][1000 genomes]
rs9314852	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	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:51 , 50 per page) page: 1 2

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	chr9:79086200-79093400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr9:79087600-79117400	Weak transcription	Colonic Mucosa	Colon
8	chr9:79087800-79093200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr9:79088200-79093200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr9:79088200-79093200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr9:79088400-79093200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:79088400-79097000	Weak transcription	Stomach Mucosa	stomach
13	chr9:79088800-79093200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:79088800-79093200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr9:79088800-79093800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr9:79089000-79100800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr9:79089000-79103400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr9:79089000-79116400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr9:79090000-79094000	Strong transcription	Osteobl	bone
20	chr9:79090400-79094200	Strong transcription	Muscle Satellite Cultured Cells	--
21	chr9:79090600-79094200	Strong transcription	Duodenum Mucosa	Duodenum
22	chr9:79091000-79093200	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr9:79091000-79093200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr9:79091200-79093200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr9:79091200-79108800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr9:79092200-79093800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr9:79092200-79093800	Strong transcription	Fetal Intestine Large	intestine
28	chr9:79092400-79093800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr9:79092400-79093800	Strong transcription	HMEC	breast
30	chr9:79092400-79093800	Strong transcription	HSMM	muscle
31	chr9:79092600-79093400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
32	chr9:79092600-79093600	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr9:79092600-79093600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
34	chr9:79092600-79093800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
35	chr9:79092600-79093800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
36	chr9:79092600-79093800	Strong transcription	Primary hematopoietic stem cells	blood
37	chr9:79092600-79094200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr9:79092800-79093400	ZNF genes & repeats	Fetal Stomach	stomach
39	chr9:79092800-79093800	ZNF genes & repeats	Primary B cells from cord blood	blood
40	chr9:79092800-79093800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr9:79093000-79093200	Weak transcription	Primary B cells from peripheral blood	blood
42	chr9:79093000-79093400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr9:79093000-79093400	ZNF genes & repeats	Lung	lung
44	chr9:79093000-79093600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr9:79093000-79093600	ZNF genes & repeats	Fetal Thymus	thymus
46	chr9:79093000-79093600	Strong transcription	NHDF-Ad	bronchial
47	chr9:79093000-79093800	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr9:79093000-79093800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
49	chr9:79093000-79093800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
50	chr9:79093000-79093800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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