Variant report

Variant	rs191965591
Chromosome Location	chr4:107084093-107084094
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879701	chr4:107024776-107163128	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv508301	chr4:107049086-107092730	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv1799357	chr4:107058025-107099737	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1801434	chr4:107058025-107099737	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1800933	chr4:107058025-107118662	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv1802243	chr4:107058025-107118662	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv1802962	chr4:107058025-107118662	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv1803376	chr4:107058025-107118662	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv1848076	chr4:107058334-107118662	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv1851828	chr4:107059549-107118662	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv879702	chr4:107065718-107175191	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv879703	chr4:107082926-107163128	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107038000-107112000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr4:107053800-107101600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr4:107054000-107091000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr4:107054000-107113600	Weak transcription	Brain Anterior Caudate	brain
5	chr4:107066400-107151200	Weak transcription	Colon Smooth Muscle	Colon
6	chr4:107070600-107084200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr4:107071800-107176400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr4:107073000-107086800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr4:107074200-107114400	Weak transcription	NHDF-Ad	bronchial
10	chr4:107074600-107111800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr4:107075200-107091000	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr4:107075800-107114000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr4:107075800-107118200	Weak transcription	Brain Substantia Nigra	brain
14	chr4:107075800-107129600	Weak transcription	Spleen	Spleen
15	chr4:107076400-107114200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr4:107077000-107089600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr4:107078000-107107800	Weak transcription	HSMMtube	muscle
18	chr4:107078200-107116000	Weak transcription	Colonic Mucosa	Colon
19	chr4:107078600-107084200	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr4:107078800-107112200	Weak transcription	Osteobl	bone
21	chr4:107078800-107114200	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr4:107082400-107085000	Strong transcription	Fetal Thymus	thymus
23	chr4:107082600-107084800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:107082600-107085600	Strong transcription	Primary B cells from cord blood	blood
25	chr4:107082800-107084200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr4:107082800-107084200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
27	chr4:107082800-107085400	Strong transcription	Primary T cells from cord blood	blood
28	chr4:107082800-107086800	Weak transcription	Fetal Heart	heart
29	chr4:107083000-107084600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr4:107083000-107084800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr4:107083000-107085000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr4:107083200-107084200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:107083200-107084200	ZNF genes & repeats	Fetal Lung	lung
34	chr4:107083200-107084200	ZNF genes & repeats	Fetal Stomach	stomach
35	chr4:107083200-107084400	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
36	chr4:107083200-107084400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
37	chr4:107083200-107084400	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr4:107083200-107085000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
39	chr4:107083200-107085200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr4:107083200-107090400	Weak transcription	Fetal Brain Male	brain
41	chr4:107083200-107173400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr4:107083400-107084200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
43	chr4:107083400-107084200	ZNF genes & repeats	Aorta	Aorta
44	chr4:107083400-107084200	ZNF genes & repeats	Fetal Muscle Leg	muscle
45	chr4:107083400-107084200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
46	chr4:107083400-107084200	Strong transcription	Skeletal Muscle Female	skeletal muscle
47	chr4:107083400-107084200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
48	chr4:107083600-107084200	ZNF genes & repeats	HepG2	liver
49	chr4:107083600-107084600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:107083600-107084600	ZNF genes & repeats	Primary B cells from peripheral blood	blood

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