Variant report

Variant	rs555723572
Chromosome Location	chr4:57784403-57784404
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:57772971..57776902-chr4:57777481..57784789,10	MCF-7	breast:
2	chr4:57776711..57779494-chr4:57781932..57784622,2	MCF-7	breast:
3	chr4:57772930..57780141-chr4:57782916..57788353,10	K562	blood:

Variant related genes	Relation type
ENSG00000084093	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv868815	chr4:57114268-58084688	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv1012287	chr4:57652778-57853485	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv1012125	chr4:57668229-57865803	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	esv3425352	chr4:57783591-57820951	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:57775800-57786200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr4:57776400-57789400	Weak transcription	Right Ventricle	heart
3	chr4:57777000-57785400	Genic enhancers	Primary T cells fromperipheralblood	blood
4	chr4:57777000-57786400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr4:57777000-57795800	Weak transcription	A549	lung
6	chr4:57777000-57796600	Weak transcription	Fetal Brain Female	brain
7	chr4:57777000-57797000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr4:57777200-57793400	Weak transcription	HMEC	breast
9	chr4:57777200-57796600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:57777200-57796600	Weak transcription	Aorta	Aorta
11	chr4:57777200-57796800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:57777200-57797200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr4:57777400-57784600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:57777400-57786200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr4:57777600-57785800	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr4:57777600-57796000	Weak transcription	Brain Anterior Caudate	brain
17	chr4:57777600-57796000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr4:57777600-57796600	Weak transcription	Colonic Mucosa	Colon
19	chr4:57777600-57803200	Weak transcription	NHDF-Ad	bronchial
20	chr4:57777600-57805600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:57777600-57806000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr4:57778000-57785600	Strong transcription	Fetal Stomach	stomach
23	chr4:57778000-57791800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr4:57778000-57796000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr4:57778000-57796000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr4:57778000-57796600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr4:57778000-57797000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr4:57778200-57785600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr4:57778200-57796200	Weak transcription	Brain Hippocampus Middle	brain
30	chr4:57778200-57796800	Weak transcription	NHLF	lung
31	chr4:57778400-57786200	Weak transcription	HSMM	muscle
32	chr4:57778400-57788600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:57778400-57795400	Weak transcription	HSMMtube	muscle
34	chr4:57778400-57796000	Weak transcription	Rectal Smooth Muscle	rectum
35	chr4:57778400-57800200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:57778400-57800200	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr4:57778400-57801000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:57778600-57785200	Strong transcription	Fetal Intestine Small	intestine
39	chr4:57778800-57795800	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr4:57779000-57804600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:57779200-57799200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr4:57779400-57785000	Weak transcription	Lung	lung
43	chr4:57779800-57789600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr4:57779800-57796000	Weak transcription	Small Intestine	intestine
45	chr4:57779800-57797600	Weak transcription	Fetal Brain Male	brain
46	chr4:57779800-57799600	Weak transcription	Right Atrium	heart
47	chr4:57780200-57793000	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr4:57780400-57800400	Strong transcription	Fetal Thymus	thymus
49	chr4:57780600-57786000	Weak transcription	Fetal Kidney	kidney
50	chr4:57780800-57795600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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