Variant report
| Variant | esv3384568 |
|---|---|
| Chromosome Location | chr2:36299713-36300290 |
| 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:23 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs17331745 | chr2:36299739-36299740 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 2 | rs562991936 | chr2:36299762-36299763 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs538221327 | chr2:36299813-36299814 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs567414389 | chr2:36299821-36299822 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs2372383 | chr2:36299836-36299837 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs185818544 | chr2:36299858-36299859 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs192009826 | chr2:36299861-36299862 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs571094031 | chr2:36299866-36299867 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs182876116 | chr2:36299986-36299987 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs550115185 | chr2:36300011-36300012 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs568621905 | chr2:36300029-36300030 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs146256346 | chr2:36300032-36300033 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs188144169 | chr2:36300113-36300114 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs12472700 | chr2:36300134-36300135 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 15 | rs534129838 | chr2:36300135-36300136 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 16 | rs558593073 | chr2:36300159-36300160 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 17 | rs577038900 | chr2:36300194-36300195 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 18 | rs544620017 | chr2:36300241-36300242 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 19 | rs34826114 | chr2:36300246-36300247 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 20 | rs376592403 | chr2:36300258-36300259 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 21 | rs17403673 | chr2:36300263-36300264 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 22 | rs17018154 | chr2:36300271-36300272 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 23 | rs542337904 | chr2:36300282-36300283 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:62)
| Disease | PMID | Source |
|---|---|---|
| Breast cancer | 17393978 | CNVD |
| Acute lymphoblastic leukemia | 21098271 | CNVD |
| Breast cancer | 17603634 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Lynch syndrome | 18415027 | CNVD |
| Basal cell lymphoma | 16317097 | CNVD |
| Diffuse large b-cell lymphoma | 16317097 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Diffuse large b-cell lymphoma | 18287131 | CNVD |
| Ovarian neoplasms | 16753589 | CNVD |
| Glioblastoma multiforme | 17387387 | CNVD |
| Neuroblastoma | 17533364 | CNVD |
| Neuroblastoma | 18923191 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Adrenal tumor | 17535989 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Basal cell lymphoma | 17053054 | CNVD |
| Medulloblastoma | 17522785 | CNVD |
| Cancer | 23418310 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Ependymoma | 16718352 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| lymphocytic leukemia | 21291569 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Bladder cancer | 21909424 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Intellectual disability | 22102821 | CNVD |
| Cancer | 20164919 | CNVD |
| Hodgkin''s lymphoma | 18641027 | CNVD |
| Autism | 22495311 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| Follicular lymphoma | 20505157 | CNVD |
| Autism | 17483303 | CNVD |
| Invasive pancreatic ductal carcinoma | 16982739 | CNVD |
| Myofibroblastic sarcoma | 19369631 | CNVD |
| Esophageal adenocarcinoma | 18519675 | CNVD |
| Medulloblastoma | 20607354 | CNVD |
| Leukemia | 18628472 | CNVD |
| Autism | 19521722 | CNVD |
| Autism | 18522746 | CNVD |
| Breast cancer | 21364760 | CNVD |
| Wilms tumour | 21544195 | CNVD |
| Non-small cell lung cancer | 18927303 | CNVD |
| Hereditary gingival fibromatosis | 19633868 | CNVD |
| Breast cancer | 21785460 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Breast cancer | 21045282 | CNVD |
| Prostate cancer | 21965145 | CNVD |
| Breast cancer | 16397240 | CNVD |
| Acute lymphoblastic leukemia | 21390130 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Neuroblastoma | 21508638 | CNVD |
| Neurodevelopmental disorder | 22521361 | CNVD |
| Neurocytoma | 17123091 | CNVD |
| Autism | 22495309 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Melanoma | 18172304 | CNVD |
| Cancer | 16751803 | CNVD |
| Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:36288400-36306400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
