Variant report
| Variant | esv3433740 |
|---|---|
| Chromosome Location | chr3:160723606-160724016 |
| 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 | rs370084877 | chr3:160723620-160723621 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs529507231 | chr3:160723690-160723691 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs185943615 | chr3:160723723-160723724 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs529965492 | chr3:160723733-160723734 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs147938515 | chr3:160723769-160723770 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs190608768 | chr3:160723770-160723771 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs530416595 | chr3:160723781-160723782 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs550677856 | chr3:160723848-160723849 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs560246433 | chr3:160723917-160723918 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs570421300 | chr3:160723926-160723927 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs75083867 | chr3:160723933-160723934 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs778662 | chr3:160723941-160723942 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 13 | rs372149425 | chr3:160723953-160723954 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs183636182 | chr3:160724009-160724010 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:58)
| Disease | PMID | Source |
|---|---|---|
| Basal cell lymphoma | 17053054 | CNVD |
| Esophageal cancer | 21851588 | CNVD |
| Uveal melanoma | 21693616 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Retinoblastoma | 21504564 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Intellectual disability | 22102821 | CNVD |
| Autism | 22495311 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Squamous cell cancer | 20885788 | CNVD |
| Melanoma | 18172304 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Breast cancer | 22032731 | CNVD |
| Breast cancer | 16461572 | CNVD |
| Neuroblastoma | 17533364 | CNVD |
| Cervical Cancer | 21857958 | CNVD |
| Melanoma | 21693616 | CNVD |
| Lung cancer | 21426551 | CNVD |
| Cancer | 21637783 | CNVD |
| Cervical cancer | 21063398 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Liposarcoma | 21253554 | CNVD |
| Oral cancer | 21386901 | CNVD |
| Renal cell carcinoma | 19461508 | CNVD |
| Cancer | 22065749 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Basal cell lymphoma | 21115979 | CNVD |
| head and neck squamous cell carcinoma | 17671120 | CNVD |
| Esophageal squamous carcinoma | 18350619 | CNVD |
| Myelodysplastic syndrome | 21251322 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Acute lymphoblastic leukemia | 21339820 | CNVD |
| Breast cancer | 16608533 | CNVD |
| Acute myeloid leukemia | 20729466 | CNVD |
| Non-small cell lung cancer | 19010865 | CNVD |
| abnormal development | 18461090 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Ovarian clear cell carcinoma | 21343371 | CNVD |
| Colorectal cancer | 16272173 | CNVD |
| Prostate cancer | 16547154 | CNVD |
| Breast cancer | 21364760 | CNVD |
| Gastrointestinal stromal cancer | 20818650 | CNVD |
| Prostate cancer | 16573809 | CNVD |
| Breast cancer | 21785460 | CNVD |
| Bladder cancer | 21909424 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Intellectual disability | 21811512 | CNVD |
| Breast cancer | 22522925 | CNVD |
| Pancreatic cancer | 17952125 | CNVD |
| Sudden cardiac death | 19188705 | CNVD |
| Mantle cell lymphoma | 19029149 | CNVD |
| Malformation | 19546859 | CNVD |
| Schizophrenia | 19546859 | CNVD |
| Breast cancer | 17133270 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:160721400-160724800 | Weak transcription | Brain Anterior Caudate | brain |
