Variant report

Variant	rs145380077
Chromosome Location	chr4:26290420-26290421
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:26281907..26283732-chr4:26289756..26291455,2	MCF-7	breast:
2	chr4:26290132..26292297-chr4:26397412..26399747,2	K562	blood:

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	nsv829889	chr4:26169954-26338313	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv519405	chr4:26284472-26292555	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv593852	chr4:26284472-26292636	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv1793856	chr4:26284472-26294886	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv1794278	chr4:26284472-26294886	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv1798961	chr4:26284472-26294886	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv593853	chr4:26286920-26295174	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv3467038	chr4:26290291-26295493	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3467039	chr4:26290345-26295472	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3467037	chr4:26290356-26295454	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv822510	chr4:26290417-26295069	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv822511	chr4:26290417-26295508	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26282000-26290800	Weak transcription	Placenta	Placenta
2	chr4:26289400-26291200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr4:26289600-26290600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:26289600-26290600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:26289600-26290800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr4:26289600-26290800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr4:26289600-26291200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:26289600-26291200	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr4:26289600-26292000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:26289600-26293000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:26289800-26290600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr4:26289800-26290600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:26289800-26290600	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr4:26289800-26290600	Enhancers	NH-A	brain
15	chr4:26289800-26290600	Enhancers	Osteobl	bone
16	chr4:26289800-26290800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr4:26289800-26291400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr4:26289800-26292000	Enhancers	NHEK	skin
19	chr4:26290000-26290600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:26290000-26290600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr4:26290000-26290600	Flanking Active TSS	NHDF-Ad	bronchial
22	chr4:26290000-26290800	Enhancers	NHLF	lung
23	chr4:26290000-26291200	Weak transcription	Colon Smooth Muscle	Colon
24	chr4:26290000-26291400	Enhancers	Primary hematopoietic stem cells	blood
25	chr4:26290000-26291400	Enhancers	HSMM	muscle
26	chr4:26290000-26291600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr4:26290000-26291600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:26290200-26290800	Weak transcription	Primary B cells from cord blood	blood
29	chr4:26290200-26290800	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr4:26290200-26291200	Weak transcription	Adipose Nuclei	Adipose
31	chr4:26290200-26291200	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr4:26290200-26291600	Weak transcription	Fetal Muscle Leg	muscle
33	chr4:26290200-26292200	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr4:26290200-26297200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:26290400-26290600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr4:26290400-26290600	Enhancers	GM12878-XiMat	blood
37	chr4:26290400-26290800	Weak transcription	Stomach Mucosa	stomach
38	chr4:26290400-26290800	Weak transcription	HMEC	breast
39	chr4:26290400-26290800	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr4:26290400-26291400	Weak transcription	Fetal Stomach	stomach
41	chr4:26290400-26291800	Weak transcription	HSMMtube	muscle

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