Variant report
Variant | esv1818175 |
---|---|
Chromosome Location | chr2:48851820-48855065 |
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 | rs6705189 | chr2:48851820-48851821 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
2 | rs539693677 | chr2:48851834-48851835 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs551552037 | chr2:48851882-48851883 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs566903339 | chr2:48851896-48851897 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs377285388 | chr2:48851902-48851903 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs76595721 | chr2:48851911-48851912 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs573722173 | chr2:48851955-48851956 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs544296196 | chr2:48851958-48851959 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs562438704 | chr2:48851976-48851977 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs532298167 | chr2:48851986-48851987 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs555747634 | chr2:48852038-48852039 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs532994937 | chr2:48852045-48852046 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs371494929 | chr2:48852059-48852060 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs183366550 | chr2:48852134-48852135 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs556740716 | chr2:48852138-48852139 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs578136949 | chr2:48852158-48852159 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs34206180 | chr2:48852178-48852179 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs545476595 | chr2:48852207-48852208 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
19 | rs545002855 | chr2:48852272-48852273 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
20 | rs572925777 | chr2:48852305-48852306 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
21 | rs540536771 | chr2:48852341-48852342 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs115397499 | chr2:48852359-48852360 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
23 | rs376630716 | chr2:48852363-48852364 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
24 | rs564797521 | chr2:48852422-48852423 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
25 | rs543803851 | chr2:48852470-48852471 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs193096945 | chr2:48852506-48852507 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs528816436 | chr2:48852531-48852532 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs532875190 | chr2:48852532-48852533 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs547279281 | chr2:48852543-48852544 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs551031424 | chr2:48852560-48852561 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs185706320 | chr2:48852562-48852563 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs141552540 | chr2:48852654-48852655 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs538811021 | chr2:48852701-48852702 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs549676791 | chr2:48852732-48852733 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs114830857 | chr2:48852743-48852744 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs538283020 | chr2:48852747-48852748 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs556605514 | chr2:48852778-48852779 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
38 | rs571622963 | chr2:48852835-48852836 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
39 | rs186512560 | chr2:48852852-48852853 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs568647336 | chr2:48852875-48852876 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs553941817 | chr2:48852907-48852908 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs145310491 | chr2:48852927-48852928 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
43 | rs540034889 | chr2:48852944-48852945 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
44 | rs191334757 | chr2:48852970-48852971 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs573845929 | chr2:48852974-48852975 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs141695870 | chr2:48852984-48852985 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
47 | rs75875980 | chr2:48853008-48853009 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
48 | rs6709346 | chr2:48853032-48853033 | ZNF genes & repeats Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
49 | rs544735239 | chr2:48853034-48853035 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
50 | rs79033228 | chr2:48853045-48853046 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Medulloblastoma | 21979893 | CNVD |
Lynch syndrome | 18415027 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Diffuse large b-cell lymphoma | 18287131 | CNVD |
Ovarian neoplasms | 16753589 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Neuroblastoma | 17533364 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Adrenal tumor | 17535989 | CNVD |
Breast cancer | 21264507 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Medulloblastoma | 17522785 | CNVD |
Cancer | 23418310 | CNVD |
Breast cancer | 17603634 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Ependymoma | 16718352 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Prostate cancer | 18632612 | CNVD |
Bladder cancer | 21909424 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Intellectual disability | 22102821 | CNVD |
Cancer | 20164919 | CNVD |
Hodgkin''s lymphoma | 18641027 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Follicular lymphoma | 20505157 | CNVD |
Autism | 17483303 | CNVD |
Myofibroblastic sarcoma | 19369631 | CNVD |
Esophageal adenocarcinoma | 18519675 | CNVD |
Medulloblastoma | 20607354 | CNVD |
Leukemia | 18628472 | CNVD |
Autism | 22495311 | CNVD |
Autism | 18522746 | CNVD |
Breast cancer | 21785460 | CNVD |
Lung cancer | 18438408 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Neuroblastoma | 21508638 | CNVD |
Neurodevelopmental disorder | 22521361 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Melanoma | 18172304 | CNVD |
Cancer | 16751803 | CNVD |
Colorectal cancer | 16272173 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Williams Syndrome | 20824207 | CNVD |
Breast cancer | 16272173 | CNVD |
Lung cancer | 17297452 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Ovarian cancer | 21720365 | CNVD |
abnormal development | 18461090 | CNVD |
Breast cancer | 21364760 | CNVD |
Schizophrenia | 20433910 | CNVD |
Autism | 21701786 | CNVD |
Attention deficit hyperactivity disorder | 21324949 | CNVD |
Austim spectrum disorder | 21302340 | CNVD |
Schizophrenia | 20587603 | CNVD |
Schizophrenia | 20553308 | CNVD |
Autism | 22241247 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Lung adenocarcinoma | 17086460 | CNVD |
Retinoblastoma | 22278416 | CNVD |
Cancer | 21183584 | CNVD |
Breast cancer | 16397240 | CNVD |
Acute lymphoblastic leukemia | 18768390 | CNVD |
Mental retardation | 19521722 | CNVD |
Schizophrenia | 18990708 | CNVD |
Schizophrenia | 18940311 | CNVD |
Schizophrenia | 19348701 | CNVD |
Schizophrenia | 18945720 | CNVD |
Schizophrenia | 19571808 | CNVD |
Prostate cancer | 16573809 | CNVD |
Neuroticism | 17667963 | CNVD |
Schizophrenia | 19443537 | CNVD |
Schizophrenia | 19546859 | CNVD |
Autism | 17322880 | CNVD |
Lung cancer | 17086460 | CNVD |
Chronic lymphocytic leukemia | 17053054 | CNVD |
Hereditary non-polyposis colorectal cancer | 19566914 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Acute lymphoblastic leukemia | 21980252 | CNVD |
Breast cancer | 22522925 | CNVD |
T-cell lymphomas | 22341440 | CNVD |
Pancreatic cancer | 17952125 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:48831000-48859600 | Weak transcription | Ovary | ovary |
2 | chr2:48836600-48862000 | Weak transcription | Stomach Smooth Muscle | stomach |
3 | chr2:48847000-48853000 | Weak transcription | Colon Smooth Muscle | Colon |
4 | chr2:48853000-48853400 | ZNF genes & repeats | Colon Smooth Muscle | Colon |
5 | chr2:48853000-48854000 | ZNF genes & repeats | Duodenum Smooth Muscle | Duodenum |
6 | chr2:48853400-48853800 | Weak transcription | Colon Smooth Muscle | Colon |
7 | chr2:48854000-48873600 | Weak transcription | Duodenum Smooth Muscle | Duodenum |