Variant report
| Variant | esv3435884 |
|---|---|
| Chromosome Location | chr2:186624082-186624424 |
| 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:14 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs146397707 | chr2:186624137-186624138 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs112174448 | chr2:186624141-186624142 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs201843432 | chr2:186624144-186624145 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs563301050 | chr2:186624216-186624217 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs59153366 | chr2:186624224-186624225 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
| 6 | rs13036018 | chr2:186624276-186624277 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs535239841 | chr2:186624277-186624278 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs201958996 | chr2:186624328-186624329 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs201721010 | chr2:186624333-186624334 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs376587227 | chr2:186624336-186624337 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs368969691 | chr2:186624337-186624338 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs528404919 | chr2:186624357-186624358 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs35750344 | chr2:186624368-186624369 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs112032214 | chr2:186624377-186624378 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:51)
| Disease | PMID | Source |
|---|---|---|
| Breast cancer | 17603634 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Ependymoma | 16718352 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Intellectual disability | 22102821 | CNVD |
| Autism | 18522746 | CNVD |
| Melanoma | 18172304 | CNVD |
| Cancer | 16751803 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Acute lymphoblastic leukemia | 20067559 | CNVD |
| Acute lymphoblastic leukemia | 21980252 | CNVD |
| Testicular germ cell tumor | 18059402 | CNVD |
| Breast cancer | 16272173 | CNVD |
| Ewing''s sarcoma | 17952124 | CNVD |
| Cancer | 21637783 | CNVD |
| Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Liposarcoma | 21253554 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Embryonal rhabdomyosarcoma | 16790082 | CNVD |
| Autism | 16446308 | CNVD |
| Autism | 19401682 | CNVD |
| Colorectal cancer | 16272173 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Glioblastoma | 21080181 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Acute myeloid leukemia | 20729466 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Facial dysmorphism | 20548289 | CNVD |
| Mental retardation | 20548289 | CNVD |
| Biliary cancer | 20360734 | CNVD |
| Breast cancer | 20360734 | CNVD |
| Coronary artery disease | 20360734 | CNVD |
| Crohn''s disease | 20360734 | CNVD |
| Hypertension | 20360734 | CNVD |
| Rheumatoid arthritis | 20360734 | CNVD |
| Type 1 diabetes | 20360734 | CNVD |
| Type 2 diabetes | 20360734 | CNVD |
| Breast cancer | 21364760 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Hirschsprung''s Disease | 21712996 | CNVD |
| Cancer | 21183584 | CNVD |
| Sudden cardiac death | 19188705 | CNVD |
| Autism | 19329560 | CNVD |
| Urothelial carcinoma | 21177765 | CNVD |
| early-passage human iPS cells | 21368824 | CNVD |
| Schizophrenia | 23813976 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:186606800-186632000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
| 2 | chr2:186613600-186635000 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
| 3 | chr2:186622400-186625800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
