Variant report
Variant | esv2246425 |
---|---|
Chromosome Location | chr8:89392008-89392721 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- 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 | rs561406006 | chr8:89392021-89392022 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs549555900 | chr8:89392032-89392033 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs567859952 | chr8:89392033-89392034 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs538535304 | chr8:89392094-89392095 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs183327317 | chr8:89392100-89392101 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs535576227 | chr8:89392119-89392120 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs186555967 | chr8:89392129-89392130 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs4961093 | chr8:89392132-89392133 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
9 | rs191191147 | chr8:89392133-89392134 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs572409506 | chr8:89392140-89392141 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs114425953 | chr8:89392166-89392167 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs115178802 | chr8:89392188-89392189 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs182704046 | chr8:89392219-89392220 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs201726746 | chr8:89392220-89392221 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs200217232 | chr8:89392222-89392223 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs369480435 | chr8:89392263-89392264 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs370119280 | chr8:89392305-89392306 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs373063061 | chr8:89392505-89392506 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
19 | rs188225145 | chr8:89392512-89392513 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
20 | rs192796688 | chr8:89392514-89392515 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
21 | rs76974387 | chr8:89392525-89392526 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs377361093 | chr8:89392528-89392529 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
23 | rs573543260 | chr8:89392593-89392594 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
24 | rs558836331 | chr8:89392598-89392599 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
25 | rs114113187 | chr8:89392630-89392631 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs185121876 | chr8:89392635-89392636 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs577889183 | chr8:89392646-89392647 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Wilms tumour | 21544195 | CNVD |
Gastric cancer | 17908304 | CNVD |
Melanoma | 18172304 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Autism | 19415332 | CNVD |
Malaria | 21533027 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Breast cancer | 21245420 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Seminomas | 18059402 | CNVD |
Autism | 22495311 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Pancreatic cancer | 21811587 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Breast cancer | 17603634 | CNVD |
Testicular cancer | 18059402 | CNVD |
Breast cancer | 17133270 | CNVD |
Breast cancer | 21509527 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Breast cancer | 21858162 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Acute lymphoblastic leukemia | 21248843 | CNVD |
Cancer | 20164919 | CNVD |
Esophageal cancer | 20955586 | CNVD |
Multiple myeloma | 16461302 | CNVD |
abnormal development | 18461090 | CNVD |
Oral cancer | 21386901 | CNVD |
Uveal melanoma | 21693616 | CNVD |
Langer-Giedion syndrome | 22283845 | CNVD |
Cancer | 21637783 | CNVD |
Splenic marginal zone lymphoma | 21957467 | CNVD |
Breast cancer | 20632083 | CNVD |
Breast cancer | 19602461 | CNVD |
Cancer | 22429812 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Oral cancer | 19627613 | CNVD |
Prostate cancer | 21088497 | CNVD |
colon cancer | 17210682 | CNVD |
Breast cancer | 21264507 | CNVD |
Breast cancer | 22028636 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Cancer | 16751803 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Gastric cancer | 17167181 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Breast cancer | 16461572 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Medulloblastoma | 16968546 | CNVD |
head and neck squamous cell carcinoma | 18028549 | CNVD |
Breast cancer | 17001317 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Lung cancer | 18438408 | CNVD |
Breast cancer | 16608533 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Prostate cancer | 18632612 | CNVD |
Glioblastoma multiforme | 18628472 | CNVD |
Ovarian cancer | 22174824 | CNVD |
Prostate cancer | 16573809 | CNVD |
Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
Cancer | 21949371 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Acute myeloid leukemia | 21358987 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Adenocarcinoma | 21044232 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
T-cell prolymphocytic leukemia | 17713554 | CNVD |
Prostate cancer | 16461572 | CNVD |
Breast cancer | 21399628 | CNVD |
Acute lymphoblastic leukemia | 18458336 | CNVD |
small cell lung cancer | 20016488 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Breast cancer | 17393978 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Non-syndromic sensorineural hearing loss | 20606397 | CNVD |
Bladder cancer | 19088036 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Breast cancer | 17899364 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Epilepsy | 20502679 | CNVD |
Breast cancer | 20409316 | CNVD |
Acute myeloid leukemia | 19651601 | CNVD |
head and neck squamous cell carcinoma | 19451471 | CNVD |
Renal cell carcinoma | 18765545 | CNVD |
Basal cell lymphoma | 17170743 | CNVD |
Cutaneous T-cell lymphoma | 21881587 | CNVD |
Breast cancer | 21611746 | CNVD |
Breast cancer | 21364760 | CNVD |
Colorectal cancer | 21645411 | CNVD |
Pancreatic cancer | 17952125 | CNVD |
Breast cancer | 22522925 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:89380600-89394800 | Weak transcription | H9 Cell Line | embryonic stem cell |
2 | chr8:89389400-89392800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr8:89391200-89393000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |