Variant report

Variant	rs145417415
Chromosome Location	chr6:33565851-33565852
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NR3C1	chr6:33565660-33566066	A549	lung:	n/a	chr6:33565849-33565870 chr6:33565853-33565867 chr6:33565861-33565870 chr6:33565853-33565867
2	REST	chr6:33565681-33565934	SK-N-SH	brain:	n/a	chr6:33565899-33565912
3	NR3C1	chr6:33565638-33566066	A549	lung:	n/a	chr6:33565849-33565870 chr6:33565853-33565867 chr6:33565861-33565870 chr6:33565853-33565867
4	NR3C1	chr6:33565760-33565949	A549	lung:	n/a	chr6:33565849-33565870 chr6:33565853-33565867 chr6:33565861-33565870 chr6:33565853-33565867

No.	Distal block	Cell Line	Cell type
1	chr6:33557038..33558663-chr6:33565418..33568204,3	K562	blood:
2	chr6:33556929..33561530-chr6:33563084..33565973,5	MCF-7	breast:
3	chr6:33559755..33561474-chr6:33565706..33568231,2	K562	blood:

Variant related genes	Relation type
LINC00336	TF binding region
ENSG00000197251	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv462896	chr6:33534880-33588147	Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv602833	chr6:33534880-33588147	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv885770	chr6:33543409-33614127	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS 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	34 gene(s)	inside rSNPs	diseases
4	nsv830638	chr6:33551202-33711346	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
5	esv992246	chr6:33561708-33570974	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv5250	chr6:33565017-33598370	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33558600-33567200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr6:33559000-33567200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:33559400-33567200	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr6:33559600-33569800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr6:33561200-33567200	Weak transcription	Left Ventricle	heart
6	chr6:33561400-33567200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:33561400-33567200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr6:33561400-33567200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:33561400-33567200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:33561400-33567200	Weak transcription	Esophagus	oesophagus
11	chr6:33561400-33567200	Weak transcription	Gastric	stomach
12	chr6:33561400-33567200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:33561400-33567200	Weak transcription	NH-A	brain
14	chr6:33561600-33567000	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr6:33561600-33567200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:33561600-33567200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr6:33561600-33567400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr6:33561600-33567400	Weak transcription	NHLF	lung
19	chr6:33561600-33570400	Weak transcription	Fetal Intestine Large	intestine
20	chr6:33563400-33567000	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr6:33563400-33567200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:33563400-33567200	Weak transcription	NHDF-Ad	bronchial
23	chr6:33563600-33567200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr6:33563600-33567200	Weak transcription	A549	lung
25	chr6:33564200-33566000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr6:33564200-33566200	Enhancers	Primary B cells from peripheral blood	blood
27	chr6:33564400-33567000	Weak transcription	Hela-S3	cervix
28	chr6:33564400-33567000	Weak transcription	NHEK	skin
29	chr6:33564400-33567800	Enhancers	Primary T cells fromperipheralblood	blood
30	chr6:33564600-33566000	Enhancers	HepG2	liver
31	chr6:33564600-33566200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr6:33564800-33566200	Enhancers	Primary T cells from cord blood	blood
33	chr6:33564800-33566200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr6:33564800-33566800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:33564800-33567400	Enhancers	Fetal Thymus	thymus
36	chr6:33565000-33566000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:33565000-33567200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr6:33565400-33566000	Enhancers	Spleen	Spleen
39	chr6:33565400-33567800	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr6:33565600-33566000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:33565600-33566000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr6:33565600-33566000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr6:33565600-33566000	Enhancers	Lung	lung
44	chr6:33565600-33566000	Enhancers	Right Ventricle	heart
45	chr6:33565600-33566000	Enhancers	HMEC	breast
46	chr6:33565600-33567200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr6:33565800-33566000	Enhancers	Fetal Intestine Small	intestine
48	chr6:33565800-33566200	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr6:33565800-33566600	Enhancers	Primary T killer memory cells from peripheral blood	blood

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