Variant report
Variant | esv3489769 |
---|---|
Chromosome Location | chr1:190051429-190055027 |
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 | rs71123067 | chr1:190053602-190053603 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs373553801 | chr1:190053603-190053604 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs200621830 | chr1:190053604-190053605 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs573698405 | chr1:190053622-190053623 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs542233161 | chr1:190053662-190053663 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs552936911 | chr1:190053689-190053690 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs188885515 | chr1:190053743-190053744 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs545756695 | chr1:190053753-190053754 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs376511903 | chr1:190053769-190053770 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs74130858 | chr1:190053790-190053791 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
11 | rs544834461 | chr1:190053841-190053842 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs552726093 | chr1:190053869-190053870 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs571099913 | chr1:190053877-190053878 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs386637907 | chr1:190053878-190053879 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs68149637 | chr1:190053879-190053880 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs112188086 | chr1:190053889-190053890 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs184507080 | chr1:190053899-190053900 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs187140602 | chr1:190053901-190053902 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs528368980 | chr1:190053956-190053957 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs551287423 | chr1:190053963-190053964 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs571096625 | chr1:190053982-190053983 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs114571244 | chr1:190054035-190054036 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs550385008 | chr1:190054041-190054042 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs567205434 | chr1:190054074-190054075 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs536355911 | chr1:190054093-190054094 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
26 | rs567178490 | chr1:190054113-190054114 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
27 | rs151089395 | chr1:190054163-190054164 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
28 | rs572843388 | chr1:190054180-190054181 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
29 | rs140015861 | chr1:190054186-190054187 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
30 | rs191646260 | chr1:190054199-190054200 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Breast cancer | 17603634 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Schizophrenia | 19415332 | CNVD |
Autism | 22495311 | CNVD |
Liposarcoma | 21253554 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Melanoma | 18172304 | CNVD |
Rett syndrome | 21593744 | CNVD |
Cancer | 20164919 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Acute lymphoblastic leukemia | 17443227 | CNVD |
Wilms tumour | 21544195 | CNVD |
Breast cancer | 17133270 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Cervical cancer | 21063398 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 20632083 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Gastrointestinal stromal cancer | 20470368 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Medulloblastoma | 21292688 | CNVD |
Phyllodes tumor | 17334353 | CNVD |
Breast cancer | 21264507 | CNVD |
Multiple myeloma | 21628407 | CNVD |
Cancer | 16751803 | CNVD |
Prostate cancer | 16705090 | CNVD |
Neuroblastoma | 19435921 | CNVD |
Breast cancer | 17850661 | CNVD |
Breast cancer | 16461572 | CNVD |
Intracranial tumor | 16823260 | CNVD |
Medulloblastoma | 18056178 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Primary mediastinal b-cell lymphoma | 17728785 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Acute lymphoblastic leukemia | 21098271 | CNVD |
Neuroblastoma | 21899760 | CNVD |
Ovarian neoplasms | 16753589 | CNVD |
Glioblastoma multiforme | 17002787 | CNVD |
Breast cancer | 21858162 | CNVD |
Non-small cell lung cancer | 21385341 | CNVD |
Acute lymphoblastic leukemia | 21980252 | CNVD |
Breast cancer | 16608533 | CNVD |
Ewing''s sarcoma | 22429812 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Breast cancer | 17001317 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Prostate cancer | 18632612 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Testicular germ cell tumor | 18059402 | CNVD |
Ependymoma | 18628472 | CNVD |
Leukemia | 18628472 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Acute lymphoblastic leukemia | 19100363 | CNVD |
Lung cancer | 18438408 | CNVD |
Breast cancer | 21509527 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Melanoma | 20688739 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Breast cancer | 21611746 | CNVD |
primary effusion lymphomas | 17116491 | CNVD |
Breast cancer | 17393978 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Breast cancer | 17899364 | CNVD |
Non-small cell lung cancer | 19010865 | CNVD |
Mental retardation | 17847001 | CNVD |
Basal cell lymphoma | 17170743 | CNVD |
Follicular lymphoma | 17170743 | CNVD |
Trisomy 5 syndrome | 21098271 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Cutaneous T-cell lymphoma | 21881587 | CNVD |
Lung adenocarcinoma | 17086460 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Chronic lymphocytic leukemia | 22228453 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:190053600-190054200 | Enhancers | Placenta | Placenta |