Variant report
Variant | esv3365541 |
---|---|
Chromosome Location | chr13:62464351-62466349 |
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)
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No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs147285218 | chr13:62464394-62464395 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs530176038 | chr13:62464396-62464397 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs17205076 | chr13:62464397-62464398 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs566979267 | chr13:62464399-62464400 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs116341476 | chr13:62464414-62464415 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs191341590 | chr13:62464418-62464419 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs144627667 | chr13:62464474-62464475 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs571112822 | chr13:62464490-62464491 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs183925168 | chr13:62464501-62464502 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs556238571 | chr13:62464553-62464554 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs1888938 | chr13:62464580-62464581 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
12 | rs77752705 | chr13:62464596-62464597 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs553802992 | chr13:62464644-62464645 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs572164438 | chr13:62464646-62464647 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs189523688 | chr13:62464655-62464656 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs147210509 | chr13:62464679-62464680 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs112220085 | chr13:62464696-62464697 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs202037112 | chr13:62464697-62464698 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs562576815 | chr13:62464701-62464702 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs538807764 | chr13:62464782-62464783 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs184904434 | chr13:62464800-62464801 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs78679973 | chr13:62464822-62464823 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs9528421 | chr13:62464848-62464849 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
24 | rs34251141 | chr13:62464908-62464909 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs560598109 | chr13:62464917-62464918 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
26 | rs74853664 | chr13:62464938-62464939 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
27 | rs9528422 | chr13:62464939-62464940 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
28 | rs77452150 | chr13:62464960-62464961 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Prostate cancer | 16705090 | CNVD |
High-proliferative meningiomas | 17937814 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Intellectual disability | 22102821 | CNVD |
Cancer | 20164919 | CNVD |
Autism | 22495311 | CNVD |
Chordoma | 21602918 | CNVD |
Bladder cancer | 21949216 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Cancer | 21637783 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Chronic lymphocytic leukemia | 21518781 | CNVD |
colon cancer | 17210682 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 21264507 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Ovarian cancer | 20844748 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Intracranial aneurysm | 19064780 | CNVD |
Breast cancer | 19287154 | CNVD |
Acute myeloid leukemia | 18379011 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Olfactory neuroblastoma | 18408657 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Ependymoma | 16718352 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Colorectal cancer | 16272173 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Gastrointestinal stromal cancer | 16982739 | CNVD |
Breast cancer | 16608533 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Ovarian cancer | 22174824 | CNVD |
Breast cancer | 17133270 | CNVD |
Myoepithelioma | 18604193 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Acute lymphoblastic leukemia | 21098271 | CNVD |
Prostate cancer | 16573809 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Paraganglioma | 21461997 | CNVD |
Pheochromocytoma | 21461997 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Prostate cancer | 17245344 | CNVD |
Prostate cancer | 18632612 | CNVD |
Colorectal cancer | 21586687 | CNVD |
Small bowel adenocarcinoma | 21586687 | CNVD |
Retinoblastoma | 19183342 | CNVD |
Developmental delay | 21147756 | CNVD |
Melanoma | 18172304 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Merkel cell carcinoma | 19020549 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Lung cancer | 18438408 | CNVD |
Non-syndromic sensorineural hearing loss | 18496225 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Breast cancer | 21858162 | CNVD |
Glioblastoma multiforme | 21922591 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Gastric cancer | 17908304 | CNVD |
Glioblastoma multiforme | 21750150 | CNVD |
Breast cancer | 17603634 | CNVD |
Cancer | 21183584 | CNVD |
Breast cancer | 17393978 | CNVD |
Splenic marginal zone lymphoma | 18492102 | CNVD |
Liposarcoma | 21253554 | CNVD |
Gastrointestinal stromal cancer | 20818650 | CNVD |
head and neck squamous cell carcinoma | 17671120 | CNVD |
Colorectal cancer | 16774939 | CNVD |
Adenoid cystic carcinoma | 17372589 | CNVD |
abnormal development | 18461090 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Chronic lymphocytic leukemia | 20421269 | CNVD |
Acute lymphoblastic leukemia | 21980252 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Anaplastic thyroid cancer | 18753363 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
Non-syndromic sensorineural hearing loss | 18451855 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:62464200-62465000 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
2 | chr13:62464400-62464800 | Enhancers | HUES64 Cell Line | embryonic stem cell |
3 | chr13:62464400-62465000 | Enhancers | HUES48 Cell Line | embryonic stem cell |
4 | chr13:62464600-62465000 | Enhancers | iPS-18 Cell Line | embryonic stem cell |