Variant report
| Variant | esv3377180 |
|---|---|
| Chromosome Location | chr5:120144709-120144940 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs561898946 | chr5:120144711-120144712 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs57185087 | chr5:120144721-120144722 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 3 | rs142057682 | chr5:120144724-120144725 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs572181000 | chr5:120144741-120144742 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs529009415 | chr5:120144745-120144746 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs181705865 | chr5:120144760-120144761 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs7715474 | chr5:120144768-120144769 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 8 | rs533204320 | chr5:120144769-120144770 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs186372026 | chr5:120144778-120144779 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs146236392 | chr5:120144800-120144801 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs375714637 | chr5:120144810-120144811 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs139339998 | chr5:120144811-120144812 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs561996978 | chr5:120144830-120144831 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs555753332 | chr5:120144840-120144841 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs189911916 | chr5:120144842-120144843 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 16 | rs535100009 | chr5:120144848-120144849 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 17 | rs141782132 | chr5:120144855-120144856 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 18 | rs561904390 | chr5:120144877-120144878 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 19 | rs182347100 | chr5:120144887-120144888 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 20 | rs545197779 | chr5:120144931-120144932 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 21 | rs562696284 | chr5:120144934-120144935 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:71)
| Disease | PMID | Source |
|---|---|---|
| Metanephric adenoma | 20802469 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Acute lymphoblastic leukemia | 17690704 | CNVD |
| Gastrointestinal stromal cancer | 16982739 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Phyllodes tumor | 17334353 | CNVD |
| Malaria | 21533027 | CNVD |
| Renal cell carcinoma | 19461508 | CNVD |
| Cancer | 20164919 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Cancer | 16751803 | CNVD |
| Intellectual disability | 22102821 | CNVD |
| Breast cancer | 17603634 | CNVD |
| Acute lymphoblastic leukemia | 20067559 | CNVD |
| Melanoma | 18172304 | CNVD |
| Glioma | 20126413 | CNVD |
| Cancer | 22429812 | CNVD |
| Cancer | 21637783 | CNVD |
| Colorectal cancer | 20709793 | CNVD |
| Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
| Liposarcoma | 21253554 | CNVD |
| Acute lymphoblastic leukemia | 21390130 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Glioblastoma multiforme | 19960244 | CNVD |
| Glioblastoma multiforme | 17387387 | CNVD |
| Breast cancer | 21858162 | CNVD |
| Leukemia | 17361228 | CNVD |
| Myelodysplastic syndrome | 18508791 | CNVD |
| 5q-syndrome | 17576883 | CNVD |
| Gastric cancer | 17908304 | CNVD |
| Lung cancer | 16740712 | CNVD |
| Oral squamous cell carcinoma | 17134496 | CNVD |
| Urothelial carcinoma | 21177765 | CNVD |
| Esophageal adenocarcinoma | 19417022 | CNVD |
| Barrett''s syndrome | 19417022 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Bipolar disorder | 18458673 | CNVD |
| Thyroid cancer | 19087340 | CNVD |
| Breast cancer | 21785460 | CNVD |
| Squamous cell cancer | 20885788 | CNVD |
| Hepatocellular carcinoma | 16750200 | CNVD |
| Neurodevelopmental disorder | 22521361 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Breast cancer | 17133270 | CNVD |
| Acute myeloid leukemia | 20729466 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Acute myeloid leukemia | 21251322 | CNVD |
| lymphocytic leukemia | 21291569 | CNVD |
| Cancer | 20164920 | CNVD |
| Myelodysplastic syndrome | 21251322 | CNVD |
| Colorectal cancer | 16272173 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Acute lymphoblastic leukemia | 22237106 | CNVD |
| Hodgkin''s lymphoma | 18641027 | CNVD |
| Multiple myeloma | 17550852 | CNVD |
| Ovarian cancer | 21720365 | CNVD |
| Salivary gland tumor | 18059337 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Renal cell carcinoma | 19377443 | CNVD |
| Prostate cancer | 16461572 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Esophageal squamous carcinoma | 17470683 | CNVD |
| Glaucoma | 21310917 | CNVD |
| Glioblastoma multiforme | 22286061 | CNVD |
| Gastrointestinal stromal cancer | 19259404 | CNVD |
| Renal cell carcinoma | 18194544 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:120143600-120144800 | Enhancers | Muscle Satellite Cultured Cells | -- |
| 2 | chr5:120143600-120145000 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
