Variant report
| Variant | esv3498157 |
|---|---|
| Chromosome Location | chr2:76526429-76528928 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
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| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr2:76524609..76526850-chr2:76529570..76531746,2 | K562 | blood: |
| No data |
| No data |
| No data |
| No data |
Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page:
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| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs567327899 | chr2:76526435-76526436 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs183171203 | chr2:76526439-76526440 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs201739246 | chr2:76526513-76526514 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs371326871 | chr2:76527146-76527147 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs376046948 | chr2:76527213-76527214 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs368596950 | chr2:76527237-76527238 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs371523566 | chr2:76527246-76527247 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs376614704 | chr2:76527441-76527442 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs372463949 | chr2:76527443-76527444 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs375816171 | chr2:76527444-76527445 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs367875889 | chr2:76527668-76527669 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs539005511 | chr2:76527675-76527676 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs371710322 | chr2:76527741-76527742 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs376290466 | chr2:76527774-76527775 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs78416093 | chr2:76528092-76528093 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 16 | rs199658090 | chr2:76528095-76528096 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 17 | rs77789809 | chr2:76528099-76528100 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 18 | rs187213829 | chr2:76528126-76528127 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 19 | rs191972175 | chr2:76528130-76528131 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 20 | rs375360060 | chr2:76528166-76528167 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 21 | rs369918954 | chr2:76528275-76528276 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 22 | rs200279426 | chr2:76528385-76528386 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 23 | rs182698478 | chr2:76528893-76528894 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:53)
| Disease | PMID | Source |
|---|---|---|
| Chronic lymphocytic leukemia | 21546498 | 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 |
| Medulloblastoma | 21979893 | CNVD |
| Breast cancer | 17603634 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Ependymoma | 16718352 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Intellectual disability | 22102821 | CNVD |
| Cancer | 20164919 | CNVD |
| Hodgkin''s lymphoma | 18641027 | CNVD |
| Follicular lymphoma | 20505157 | CNVD |
| Autism | 17483303 | CNVD |
| Myofibroblastic sarcoma | 19369631 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Esophageal adenocarcinoma | 18519675 | CNVD |
| Medulloblastoma | 20607354 | CNVD |
| Autism | 22495311 | CNVD |
| Autism | 18522746 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Neurodevelopmental disorder | 22521361 | CNVD |
| Melanoma | 18172304 | CNVD |
| Cancer | 16751803 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Acute lymphoblastic leukemia | 20067559 | CNVD |
| Acute lymphoblastic leukemia | 21980252 | CNVD |
| Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
| Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
| Seminomas | 18059402 | CNVD |
| Testicular germ cell tumor | 18059402 | CNVD |
| Myeloproliferative neoplasm | 20015882 | CNVD |
| Renal cell carcinoma | 18765545 | CNVD |
| Myxofibrosarcoma | 16751306 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Acute myeloid leukemia | 21251322 | CNVD |
| Mental retardation | 17124404 | CNVD |
| Basal cell lymphoma | 19029149 | CNVD |
| Diffuse large b-cell lymphoma | 19029149 | CNVD |
| Cancer | 17440070 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Attention deficit hyperactivity disorder | 21324949 | CNVD |
| Breast cancer | 16272173 | CNVD |
| Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:76526400-76532400 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
