Variant report
Variant | esv3390304 |
---|---|
Chromosome Location | chr5:35714129-35714525 |
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 | rs111326693 | chr5:35714130-35714131 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs377652181 | chr5:35714131-35714132 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs181634222 | chr5:35714143-35714144 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs185859332 | chr5:35714145-35714146 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs79358042 | chr5:35714154-35714155 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs77721370 | chr5:35714156-35714157 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs199545847 | chr5:35714158-35714159 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs74784694 | chr5:35714163-35714164 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs370908938 | chr5:35714166-35714167 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs544214296 | chr5:35714167-35714168 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs75372630 | chr5:35714171-35714172 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs79176451 | chr5:35714172-35714173 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs76455675 | chr5:35714179-35714180 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs371426668 | chr5:35714180-35714181 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs76163707 | chr5:35714181-35714182 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs79882990 | chr5:35714191-35714192 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs368752016 | chr5:35714193-35714194 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs370071143 | chr5:35714194-35714195 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
19 | rs7723050 | chr5:35714231-35714232 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
20 | rs7726714 | chr5:35714258-35714259 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
21 | rs191044045 | chr5:35714266-35714267 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs561973518 | chr5:35714272-35714273 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
23 | rs530992448 | chr5:35714299-35714300 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
24 | rs10067994 | chr5:35714338-35714339 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
25 | rs183271191 | chr5:35714362-35714363 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs533626090 | chr5:35714365-35714366 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs78006390 | chr5:35714370-35714371 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs566820828 | chr5:35714372-35714373 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs34591551 | chr5:35714407-35714408 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs73747904 | chr5:35714439-35714440 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
31 | rs73747905 | chr5:35714479-35714480 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
32 | rs367713008 | chr5:35714487-35714488 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Myofibroblastic sarcoma | 19369631 | CNVD |
Cervical squamous cell carcinoma | 21590768 | CNVD |
Non-small cell lung cancer | 20864512 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Medulloblastoma | 16783165 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Liposarcoma | 21253554 | CNVD |
Pancreatic endocrine tumor | 17639061 | CNVD |
Cervical Cancer | 21857958 | CNVD |
Cervical cancer | 21062161 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Oral cancer | 21386901 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 21264507 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Malignant mesothelioma | 18160781 | CNVD |
Pleural malignant mesothelioma | 18160781 | CNVD |
Cervical cancer | 18559093 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Gastrointestinal stromal cancer | 16982739 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Phyllodes tumor | 17334353 | CNVD |
Malaria | 21533027 | CNVD |
Renal cell carcinoma | 19461508 | CNVD |
Colorectal cancer | 21645411 | CNVD |
Gastric cancer | 22152101 | CNVD |
Oesophago-gastric ulcer | 22152101 | CNVD |
Ovarian cancer | 21781307 | CNVD |
Breast cancer | 20668451 | CNVD |
Cancer | 20668451 | CNVD |
Lung cancer | 20668451 | CNVD |
Ovarian cancer | 20668451 | CNVD |
Pancreas cancer | 20668451 | CNVD |
Prostate cancer | 20668451 | CNVD |
Cancer | 20164919 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Multiple myeloma | 17550852 | CNVD |
prenatal diagnosis | 22389664 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Bladder cancer | 21909424 | CNVD |
DNA damage stimulus | 22844521 | CNVD |
DNA repair | 22844521 | CNVD |
Breast cancer | 21785460 | CNVD |
Spinal muscular atrophy | 22422766 | CNVD |
Spinal muscular atrophy | 22558076 | CNVD |
Spinal muscular atrophy | 21320981 | CNVD |
Spinal muscular atrophy | 21762474 | CNVD |
Breast cancer | 21858162 | CNVD |
Esophageal adenocarcinoma | 19417022 | CNVD |
Cancer | 16751803 | CNVD |
Breast cancer | 16608533 | CNVD |
Autism | 22495311 | CNVD |
Melanoma | 18172304 | CNVD |
Non-syndromic sensorineural hearing loss | 20606397 | CNVD |
Intellectual disability | 22102821 | CNVD |
Prostate cancer | 21965145 | CNVD |
Cancer | 21183584 | CNVD |
Ovarian cancer | 20844748 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Breast cancer | 17603634 | CNVD |
Non-small cell lung cancer | 19010865 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Ovarian cancer | 21720365 | CNVD |
Lung cancer | 18438408 | CNVD |
Glioma | 20126413 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
Breast cancer | 22032731 | CNVD |
Esophageal cancer | 20955586 | CNVD |
Prostate cancer | 18632612 | CNVD |
Medulloblastoma | 19270706 | CNVD |
Breast cancer | 19553991 | CNVD |
Lung cancer | 19553991 | CNVD |
Melanoma | 19553991 | CNVD |
Ovarian cancer | 19553991 | CNVD |
Prostate cancer | 19553991 | CNVD |
Non-small cell lung cancer | 17156491 | CNVD |
Breast cancer | 17133270 | CNVD |
Congenital anomalies of the kidney and urinary tract | 18694510 | CNVD |
Breast cancer | 17393978 | CNVD |
Pleomorphic liposarcoma | 18784837 | CNVD |
Acute lymphoblastic leukemia | 17640729 | CNVD |
Invasive pancreatic ductal carcinoma | 16982739 | CNVD |
Lung cancer | 19153074 | CNVD |
Breast cancer | 21364760 | CNVD |
Cornelia de Lange syndrome | 21085971 | CNVD |
Autism | 21701786 | CNVD |
Cervical cancer | 16585170 | CNVD |
Ovarian clear cell carcinoma | 19293255 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Breast cancer | 22522925 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:35697000-35717000 | Weak transcription | Left Ventricle | heart |
2 | chr5:35699400-35720600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |