Variant report

Variant	rs564589707
Chromosome Location	chr4:56215174-56215175
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:56209954..56216628-chr4:56219638..56226284,12	MCF-7	breast:
2	chr4:56211148..56230966-chr4:56256626..56269458,54	MCF-7	breast:
3	chr4:56211281..56215987-chr4:56257992..56268538,18	K562	blood:
4	chr4:56212201..56215605-chr4:56218401..56220453,4	MCF-7	breast:
5	chr4:56210683..56216526-chr4:56216680..56221548,10	K562	blood:
6	chr4:56211242..56218739-chr4:56258356..56267013,28	MCF-7	breast:
7	chr4:56213251..56215609-chr4:56227634..56229656,2	MCF-7	breast:
8	chr4:56211096..56216124-chr4:56256262..56265067,20	K562	blood:

No data

Variant related genes	Relation type
ENSG00000251111	Chromatin interaction
ENSG00000134851	Chromatin interaction
ENSG00000128039	Chromatin interaction
ENSG00000249700	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526344	chr4:55522488-56231119	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	esv3328582	chr4:56164136-56486156	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv966270	chr4:56215138-56221281	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56213200-56219000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:56213200-56230000	Weak transcription	Fetal Kidney	kidney
3	chr4:56213400-56215200	Enhancers	Fetal Lung	lung
4	chr4:56213400-56215200	Enhancers	Stomach Mucosa	stomach
5	chr4:56213400-56215200	Enhancers	NHDF-Ad	bronchial
6	chr4:56213400-56215200	Enhancers	Osteobl	bone
7	chr4:56213400-56215400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:56213400-56217000	Weak transcription	Fetal Stomach	stomach
9	chr4:56213400-56217200	Weak transcription	Lung	lung
10	chr4:56213400-56223800	Weak transcription	Fetal Heart	heart
11	chr4:56213400-56225400	Weak transcription	Spleen	Spleen
12	chr4:56213400-56233600	Weak transcription	Fetal Intestine Large	intestine
13	chr4:56213600-56215200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:56213600-56215200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:56213600-56219200	Weak transcription	Primary T cells from cord blood	blood
16	chr4:56213600-56221600	Weak transcription	HMEC	breast
17	chr4:56213600-56223000	Weak transcription	Esophagus	oesophagus
18	chr4:56213600-56223000	Weak transcription	HSMM	muscle
19	chr4:56213600-56224000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr4:56213600-56225600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr4:56213600-56229200	Weak transcription	Fetal Intestine Small	intestine
22	chr4:56213600-56230200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:56213600-56230200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:56213600-56242600	Weak transcription	Gastric	stomach
25	chr4:56213800-56217800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:56213800-56218600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr4:56213800-56221600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:56213800-56223000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr4:56213800-56225200	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr4:56213800-56225600	Weak transcription	Left Ventricle	heart
31	chr4:56213800-56227000	Weak transcription	Placenta	Placenta
32	chr4:56213800-56229800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr4:56213800-56229800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr4:56213800-56229800	Weak transcription	Fetal Muscle Trunk	muscle
35	chr4:56213800-56231800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr4:56213800-56233600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr4:56213800-56239000	Weak transcription	Brain Germinal Matrix	brain
38	chr4:56213800-56251400	Weak transcription	Pancreas	Pancrea
39	chr4:56214000-56215200	Enhancers	Brain Hippocampus Middle	brain
40	chr4:56214000-56215200	Enhancers	Hela-S3	cervix
41	chr4:56214000-56215200	Enhancers	NHLF	lung
42	chr4:56214000-56217400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:56214000-56223400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr4:56214000-56224600	Weak transcription	Primary B cells from peripheral blood	blood
45	chr4:56214000-56225600	Weak transcription	Fetal Muscle Leg	muscle
46	chr4:56214000-56229800	Weak transcription	Liver	Liver
47	chr4:56214000-56229800	Weak transcription	Fetal Thymus	thymus
48	chr4:56214000-56229800	Weak transcription	Thymus	Thymus
49	chr4:56214000-56230200	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr4:56214000-56231000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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