Variant report

Variant	rs373045598
Chromosome Location	chr4:6894793-6894794
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:6885538..6887515-chr4:6893779..6896691,2	MCF-7	breast:
2	chr4:6734514..6737444-chr4:6894118..6897087,2	K562	blood:
3	chr4:6891115..6895158-chr4:6915729..6918708,4	K562	blood:
4	chr4:6894128..6894976-chr8:99305696..99306577,2	NB4	blood:
5	chr4:6889897..6899719-chr4:6906701..6919549,30	K562	blood:
6	chr4:6886066..6889013-chr4:6893099..6895187,2	K562	blood:
7	chr4:6892678..6895514-chr4:6919772..6922371,2	K562	blood:
8	chr4:6891733..6899525-chr4:6905110..6914778,23	K562	blood:
9	chr4:6889053..6892272-chr4:6892737..6895879,4	K562	blood:
10	chr4:6893893..6894818-chr4:7072137..7072790,2	MCF-7	breast:
11	chr4:6883009..6885178-chr4:6892808..6895702,2	K562	blood:
12	chr4:6894765..6897271-chr4:7068956..7071796,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000104361	Chromatin interaction
ENSG00000132405	Chromatin interaction
ENSG00000109519	Chromatin interaction

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	nsv4216	chr4:6876592-6915629	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv878529	chr4:6883012-6983677	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers 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	30 gene(s)	inside rSNPs	diseases
3	nsv878530	chr4:6888932-7058473	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv3491705	chr4:6894126-6901649	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	esv3491706	chr4:6894126-6901649	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	esv3485871	chr4:6894726-6896135	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	esv3485873	chr4:6894729-6896245	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	esv3485870	chr4:6894758-6896269	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	esv3466977	chr4:6894765-6896148	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	esv3466978	chr4:6894765-6896148	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	esv3485872	chr4:6894781-6896099	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	esv3485874	chr4:6894788-6896141	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:6890400-6895200	Weak transcription	Pancreas	Pancrea
2	chr4:6891400-6896000	Enhancers	Primary hematopoietic stem cells	blood
3	chr4:6891800-6894800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr4:6892000-6895600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr4:6892600-6894800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr4:6892600-6895400	Enhancers	Lung	lung
7	chr4:6893000-6895800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr4:6893200-6894800	Enhancers	Fetal Muscle Leg	muscle
9	chr4:6893200-6894800	Enhancers	NHDF-Ad	bronchial
10	chr4:6893200-6895000	Enhancers	Spleen	Spleen
11	chr4:6893200-6895400	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr4:6893200-6895400	Enhancers	Fetal Thymus	thymus
13	chr4:6893200-6895400	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr4:6893400-6894800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr4:6893400-6894800	Enhancers	Fetal Stomach	stomach
16	chr4:6893400-6894800	Flanking Active TSS	K562	blood
17	chr4:6893400-6894800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr4:6893400-6895000	Enhancers	NHLF	lung
19	chr4:6893400-6895400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr4:6893400-6895400	Flanking Active TSS	HepG2	liver
21	chr4:6893400-6895400	Enhancers	NH-A	brain
22	chr4:6893400-6895600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr4:6893400-6896400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr4:6893400-6896800	Enhancers	Fetal Intestine Small	intestine
25	chr4:6893400-6897000	Enhancers	Fetal Intestine Large	intestine
26	chr4:6893600-6894800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:6893600-6894800	Enhancers	Fetal Lung	lung
28	chr4:6893600-6894800	Flanking Active TSS	A549	lung
29	chr4:6893600-6894800	Enhancers	HSMMtube	muscle
30	chr4:6893600-6895000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr4:6893600-6895600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr4:6893600-6895800	Enhancers	Fetal Kidney	kidney
33	chr4:6893800-6894800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:6893800-6894800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:6893800-6894800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr4:6893800-6894800	Enhancers	Left Ventricle	heart
37	chr4:6893800-6895400	Flanking Active TSS	Liver	Liver
38	chr4:6893800-6895400	Enhancers	Small Intestine	intestine
39	chr4:6893800-6895600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:6893800-6895600	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr4:6893800-6896800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:6894000-6894800	Enhancers	Brain Cingulate Gyrus	brain
43	chr4:6894000-6894800	Enhancers	NHEK	skin
44	chr4:6894000-6895400	Enhancers	Gastric	stomach
45	chr4:6894000-6895600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:6894200-6894800	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr4:6894200-6894800	Enhancers	Brain Substantia Nigra	brain
48	chr4:6894400-6894800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:6894400-6894800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:6894400-6894800	Enhancers	Primary T killer memory cells from peripheral blood	blood

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