Variant report

Variant	rs73666625
Chromosome Location	chr9:108062449-108062450
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:108053113..108055212-chr9:108060978..108062866,2	MCF-7	breast:
2	chr9:108061298..108064082-chr9:108078853..108080505,2	K562	blood:
3	chr9:108044800..108047623-chr9:108061922..108064222,3	MCF-7	breast:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs12341869	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28688962	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57877883	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59290851	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6479300	0.97[AFR][1000 genomes]
rs6479301	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6479302	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6479303	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6479304	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7024012	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7026389	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7033929	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7039638	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7046185	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7048497	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72744219	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs72744225	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73510211	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73510218	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73510246	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73510280	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73510281	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73510289	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73510295	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73666622	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73666624	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7847744	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7847952	0.91[AFR][1000 genomes]
rs7853038	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7853709	0.83[AMR][1000 genomes]
rs7854064	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7854282	1.00[AMR][1000 genomes]
rs7857088	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7860356	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7869261	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7873924	0.83[AMR][1000 genomes]
rs7874307	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9777083	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045108	chr9:107509553-108188550	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv831678	chr9:107923522-108112813	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv893685	chr9:107940737-108083485	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv893686	chr9:107968330-108083485	Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv893687	chr9:107973277-108083485	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv893688	chr9:107974761-108083485	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv893689	chr9:107978563-108130606	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv893690	chr9:107992706-108083485	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1037750	chr9:108027692-108251733	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108049400-108074200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr9:108053000-108063000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:108054000-108065400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:108054000-108070000	Weak transcription	Gastric	stomach
5	chr9:108054600-108090800	Weak transcription	Psoas Muscle	Psoas
6	chr9:108055200-108065000	Weak transcription	Primary B cells from cord blood	blood
7	chr9:108055600-108151200	Weak transcription	Esophagus	oesophagus
8	chr9:108056800-108077800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr9:108057000-108064200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr9:108057000-108066800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr9:108057400-108082600	Weak transcription	Dnd41	blood
12	chr9:108058200-108062600	Enhancers	NHDF-Ad	bronchial
13	chr9:108058200-108063000	Enhancers	Stomach Mucosa	stomach
14	chr9:108059200-108065800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr9:108059400-108062800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr9:108059400-108081200	Weak transcription	Fetal Kidney	kidney
17	chr9:108059800-108062600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr9:108060000-108075000	Weak transcription	Ovary	ovary
19	chr9:108060200-108077000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr9:108060400-108068200	Weak transcription	Fetal Heart	heart
21	chr9:108060600-108071000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr9:108060800-108062600	Enhancers	NH-A	brain
23	chr9:108061000-108062600	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr9:108061000-108062600	Enhancers	HMEC	breast
25	chr9:108061000-108062600	Enhancers	HSMMtube	muscle
26	chr9:108061000-108062600	Enhancers	K562	blood
27	chr9:108061000-108062800	Enhancers	HSMM	muscle
28	chr9:108061000-108069600	Weak transcription	Fetal Brain Male	brain
29	chr9:108061200-108062600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:108061200-108062600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr9:108061200-108062600	Strong transcription	Duodenum Smooth Muscle	Duodenum
32	chr9:108061200-108062600	Genic enhancers	Fetal Intestine Large	intestine
33	chr9:108061200-108062800	Genic enhancers	Fetal Intestine Small	intestine
34	chr9:108061200-108062800	Enhancers	Small Intestine	intestine
35	chr9:108061200-108063000	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:108061200-108063400	Genic enhancers	Brain Hippocampus Middle	brain
37	chr9:108061200-108066400	Strong transcription	Primary T cells from cord blood	blood
38	chr9:108061400-108062600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr9:108061400-108062600	Strong transcription	Adipose Nuclei	Adipose
40	chr9:108061400-108062600	Strong transcription	Fetal Thymus	thymus
41	chr9:108061400-108062600	Strong transcription	Left Ventricle	heart
42	chr9:108061400-108062800	Genic enhancers	HUES48 Cell Line	embryonic stem cell
43	chr9:108061400-108062800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr9:108061400-108062800	Strong transcription	Fetal Muscle Leg	muscle
45	chr9:108061400-108063000	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr9:108061400-108063600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr9:108061400-108063800	Strong transcription	Fetal Lung	lung
48	chr9:108061400-108064000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:108061600-108062600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:108061600-108062600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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