Variant report
| Variant | esv3458846 |
|---|---|
| Chromosome Location | chr2:186259951-186260394 |
| 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:15 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs114512114 | chr2:186259971-186259972 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs545987195 | chr2:186259982-186259983 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs570695549 | chr2:186260035-186260036 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs116488335 | chr2:186260045-186260046 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs190313677 | chr2:186260183-186260184 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs182240703 | chr2:186260184-186260185 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs552363300 | chr2:186260208-186260209 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs570627754 | chr2:186260235-186260236 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs554501246 | chr2:186260246-186260247 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs17403310 | chr2:186260251-186260252 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs186034020 | chr2:186260263-186260264 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs556367034 | chr2:186260285-186260286 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs565215946 | chr2:186260319-186260320 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs577093538 | chr2:186260322-186260323 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs541274386 | chr2:186260351-186260352 | 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 |
| low-grade B-cell lymphoma tumor | 18367492 | 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 |
| Autism | 22543975 | CNVD |
| Urothelial carcinoma | 21177765 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:186259800-186261200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
