Variant report

Variant	rs73409588
Chromosome Location	chr9:7107478-7107479
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs60445319	0.84[AFR][1000 genomes]
rs73407474	0.84[AFR][1000 genomes]
rs73409561	0.84[AFR][1000 genomes]
rs73409572	0.84[AFR][1000 genomes]
rs73409575	0.84[AFR][1000 genomes]
rs73409582	1.00[AFR][1000 genomes]
rs73409583	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892166	chr9:6602821-7222495	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1023906	chr9:6731786-7372132	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv613259	chr9:7032776-7541338	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers 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	4 gene(s)	inside rSNPs	diseases
4	nsv1015874	chr9:7048807-7434890	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv539971	chr9:7048807-7434890	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv869932	chr9:7068359-7133384	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv892189	chr9:7091968-7150997	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv892190	chr9:7094860-7186074	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7012200-7111200	Weak transcription	Colonic Mucosa	Colon
2	chr9:7088800-7128000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr9:7098600-7118000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:7098800-7108400	Weak transcription	HSMMtube	muscle
5	chr9:7100800-7120200	Strong transcription	Primary B cells from cord blood	blood
6	chr9:7102800-7114000	Strong transcription	Primary T cells from cord blood	blood
7	chr9:7103000-7110200	Strong transcription	Primary T helper cells fromperipheralblood	blood
8	chr9:7103000-7148600	Strong transcription	Primary B cells from peripheral blood	blood
9	chr9:7103200-7108200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr9:7103200-7108200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr9:7103200-7116200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr9:7103600-7118600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:7103800-7128800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr9:7104000-7117800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr9:7104000-7121200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr9:7104200-7117800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr9:7104200-7118000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr9:7104200-7118000	Weak transcription	HMEC	breast
19	chr9:7104200-7123600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr9:7104200-7128200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr9:7104200-7148200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr9:7104400-7113000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr9:7104400-7121200	Weak transcription	Esophagus	oesophagus
24	chr9:7104400-7121200	Weak transcription	Pancreas	Pancrea
25	chr9:7104400-7123600	Weak transcription	Gastric	stomach
26	chr9:7104400-7128000	Weak transcription	Aorta	Aorta
27	chr9:7104400-7128000	Weak transcription	Lung	lung
28	chr9:7104400-7135400	Weak transcription	Fetal Muscle Leg	muscle
29	chr9:7104400-7137600	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr9:7104400-7144600	Weak transcription	Brain Anterior Caudate	brain
31	chr9:7104600-7148000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr9:7104800-7112200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr9:7104800-7115400	Weak transcription	Brain Substantia Nigra	brain
34	chr9:7104800-7117800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr9:7104800-7120000	Weak transcription	Small Intestine	intestine
36	chr9:7104800-7123400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr9:7104800-7138200	Weak transcription	HSMM	muscle
38	chr9:7104800-7142800	Weak transcription	Osteobl	bone
39	chr9:7104800-7153200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr9:7105000-7108000	Weak transcription	Fetal Intestine Small	intestine
41	chr9:7105000-7110600	Weak transcription	Left Ventricle	heart
42	chr9:7105000-7116600	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr9:7105000-7118600	Weak transcription	Placenta	Placenta
44	chr9:7105000-7121400	Weak transcription	Spleen	Spleen
45	chr9:7105000-7133600	Weak transcription	Fetal Stomach	stomach
46	chr9:7105000-7146600	Weak transcription	Rectal Smooth Muscle	rectum
47	chr9:7105200-7108600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr9:7105200-7117800	Weak transcription	NHDF-Ad	bronchial
49	chr9:7105200-7123800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr9:7105200-7130200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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