Variant report
Variant | esv3332106 |
---|---|
Chromosome Location | chr11:5064960-5065552 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:8)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:8 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | CEBPB | chr11:5064651-5065002 | IMR90 | lung: | n/a | n/a |
2 | CEBPB | chr11:5064630-5064974 | Hela-S3 | cervix: | n/a | n/a |
3 | FOS | chr11:5064630-5064973 | MCF10A-Er-Src | breast: | n/a | n/a |
4 | FOS | chr11:5064612-5065090 | MCF10A-Er-Src | breast: | n/a | n/a |
5 | FOS | chr11:5064613-5064996 | MCF10A-Er-Src | breast: | n/a | n/a |
6 | FOS | chr11:5064601-5064986 | MCF10A-Er-Src | breast: | n/a | n/a |
7 | POLR2A | chr11:5065090-5065103 | MCF10A-Er-Src | breast: | n/a | n/a |
8 | STAT3 | chr11:5065426-5065430 | MCF10A-Er-Src | breast: | n/a | n/a |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
OR52J3 | TF binding region |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs377226305 | chr11:5065009-5065010 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
2 | rs386750096 | chr11:5065015-5065016 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
3 | rs573329673 | chr11:5065016-5065017 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
4 | rs386750097 | chr11:5065038-5065039 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
5 | rs562482539 | chr11:5065040-5065041 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
6 | rs2500002 | chr11:5065048-5065049 | Inactive region | TF binding region | 1 gene(s) | LD-proxies of rSNPOverlapped rCNV | n/a |
7 | rs77181784 | chr11:5065061-5065062 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
8 | rs2500003 | chr11:5065074-5065075 | Inactive region | TF binding region | 1 gene(s) | LD-proxies of rSNPOverlapped rCNV | n/a |
9 | rs186330785 | chr11:5065091-5065092 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
10 | rs562346573 | chr11:5065426-5065427 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Neuroblastoma | 18923191 | CNVD |
Breast cancer | 19432969 | CNVD |
Alzheimer''s disease | 17576883 | CNVD |
Long-qt syndrome | 17576883 | CNVD |
Emphysema | 19352772 | CNVD |
Invasive pancreatic ductal carcinoma | 16982739 | CNVD |
Chordoma | 18071362 | CNVD |
Breast cancer | 16608533 | CNVD |
Cancer | 21183584 | CNVD |
Gastric adenocarcinoma | 19115996 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Burkitt''s lymphoma | 19759907 | CNVD |
Breast cancer | 17603634 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Melanoma | 18172304 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Wilms tumour | 21544195 | CNVD |
Parathyroid adenoma | 22454399 | CNVD |
Chordoma | 21602918 | CNVD |
Breast cancer | 21949216 | CNVD |
Cancer | 21637783 | CNVD |
Non-syndromic sensorineural hearing loss | 19222835 | CNVD |
T-cell acute lymphoblastic leukemia | 20065082 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 21264507 | CNVD |
Beckwith-Wiedemann syndrome | 21518781 | CNVD |
Wilms tumour | 21518781 | CNVD |
Hepatoblastoma | 21518781 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Gastrointestinal stromal cancer | 17535989 | CNVD |
Paraganglioma | 17535989 | CNVD |
Pulmonary chondroma | 17535989 | CNVD |
Gastric cancer | 17908304 | CNVD |
Barrett''s syndrome | 19417022 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Multiple myeloma | 20724749 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Lung cancer | 18438408 | CNVD |
Autism | 22495311 | CNVD |
Esophageal adenocarcinoma | 18519675 | CNVD |
Ovine squamous-cell carcinoma | 17599052 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Glioma | 17123091 | CNVD |
Lung cancer | 16773561 | CNVD |
Neuroblastoma | 21124317 | CNVD |
Lung adenocarcinoma | 17086460 | CNVD |
Lung cancer | 17086460 | CNVD |
Schizophrenia | 21399695 | CNVD |
Gastric cancer | 16891809 | CNVD |
Cancer | 17160897 | CNVD |
Multiple myeloma | 16616336 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Breast cancer | 21364760 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |