Variant report
Variant | esv3320032 |
---|---|
Chromosome Location | chr1:58743468-58745149 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:58740800..58743267-chr1:58744921..58746475,2 | K562 | blood: |
No data |
No data |
No data |
No data |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs556747414 | chr1:58743489-58743490 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs567340119 | chr1:58743494-58743495 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs4912316 | chr1:58743499-58743500 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
4 | rs183157401 | chr1:58743547-58743548 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs141432028 | chr1:58743566-58743567 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs541279654 | chr1:58743594-58743595 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs189237892 | chr1:58743598-58743599 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs115368319 | chr1:58743618-58743619 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs58628857 | chr1:58743662-58743663 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs543782517 | chr1:58743738-58743739 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs375721293 | chr1:58743842-58743843 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs557188651 | chr1:58743869-58743870 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs201368287 | chr1:58743914-58743915 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs201965010 | chr1:58743915-58743916 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs563657004 | chr1:58743928-58743929 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs370742211 | chr1:58744393-58744394 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs555340067 | chr1:58744395-58744396 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs190733402 | chr1:58744568-58744569 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
19 | rs377179727 | chr1:58744822-58744823 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
20 | rs575425691 | chr1:58744921-58744922 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
21 | rs375046662 | chr1:58744993-58744994 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs542886525 | chr1:58745085-58745086 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
23 | rs559551912 | chr1:58745088-58745089 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
24 | rs117388414 | chr1:58745146-58745147 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Papillary thyroid carcinoma | 21436994 | CNVD |
Adenoid cystic carcinoma | 18698036 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Wilms tumour | 21544195 | CNVD |
Coronary Disease | 20032323 | CNVD |
Prostate cancer | 21965145 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Stargardt''s disease | 17277736 | CNVD |
Neuroblastoma | 17897457 | CNVD |
Uveal melanoma | 21693616 | CNVD |
Cancer | 21637783 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Neuroblastoma | 21484798 | CNVD |
Non-syndromic sensorineural hearing loss | 22290220 | CNVD |
Liposarcoma | 21253554 | CNVD |
Breast cancer | 21264507 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Astrocytoma | 17387387 | CNVD |
Cancer | 21499728 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Oligodendroglial tumors | 17285580 | CNVD |
Neuroblastoma | 17535989 | CNVD |
Pheochromocytoma | 17535989 | CNVD |
Prostate cancer | 16705090 | CNVD |
Astrocytoma | 17934521 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Neuroblastoma | 18664255 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Gastrointestinal stromal cancer | 19259404 | CNVD |
Gastrointestinal stromal cancer | 20470368 | CNVD |
Gastrointestinal stromal cancer | 17535989 | CNVD |
Neuroblastoma | 17533364 | CNVD |
Paraganglioma | 17535989 | CNVD |
Pulmonary chondroma | 17535989 | CNVD |
Myofibroblastic sarcoma | 19369631 | CNVD |
Breast cancer | 17603634 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Schizophrenia | 19415332 | CNVD |
Non-syndromic sensorineural hearing loss | 21030649 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Autism | 22495311 | CNVD |
Non-small cell lung cancer | 21385341 | CNVD |
Gastrointestinal stromal cancer | 16982739 | CNVD |
Chordoma | 21602918 | CNVD |
Acute lymphoblastic leukemia | 17443227 | CNVD |
Melanoma | 18172304 | CNVD |
Multiple myeloma | 16461302 | CNVD |
Melanoma | 17363583 | CNVD |
Cancer | 21129771 | CNVD |
Autosomal dominant nocturnal frontal lobe epilepsy | 18472482 | CNVD |
Hirschsprung''s Disease | 21712996 | CNVD |
Non-small cell lung cancer | 20864512 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Thrombocytopenia-absent radius syndrome | 21933853 | CNVD |
Psychiatric disorder | 22848183 | CNVD |
Diffuse large b-cell lymphoma | 18287131 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Breast cancer | 20409316 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Lung cancer | 18438408 | CNVD |
Splenic marginal zone lymphoma | 21957467 | CNVD |
Breast cancer | 17393978 | CNVD |
Cervical cancer | 21062161 | CNVD |
Cancer | 21183584 | CNVD |
Breast cancer | 21785460 | CNVD |
Breast cancer | 21364760 | CNVD |
Rett syndrome | 21593744 | CNVD |
Meckel-Gruber syndrome | 21572526 | CNVD |
Breast cancer | 16620391 | CNVD |
Multiple myeloma | 16616336 | CNVD |
Malignant mesothelioma | 18160781 | CNVD |
Pleural malignant mesothelioma | 18160781 | CNVD |
head and neck squamous cell carcinoma | 17671120 | CNVD |
Prostate cancer | 16573809 | CNVD |
Breast cancer | 16608533 | CNVD |
Breast cancer | 21509527 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Ovarian cancer | 21720365 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Developmental delay | 21147756 | CNVD |
Cancer | 20164920 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Breast cancer | 22522925 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:58724000-58759600 | Weak transcription | Ovary | ovary |
2 | chr1:58741800-58749600 | Weak transcription | Skeletal Muscle Female | skeletal muscle |