Variant report
Variant | nsv981632 |
---|---|
Chromosome Location | chr7:53209832-53219392 |
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 | rs147658330 | chr7:53214015-53214016 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs74388514 | chr7:53214021-53214022 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs12666987 | chr7:53214038-53214039 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs564693901 | chr7:53214059-53214060 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs10249672 | chr7:53214086-53214087 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
6 | rs189655756 | chr7:53214124-53214125 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs57826882 | chr7:53214127-53214128 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
8 | rs529549819 | chr7:53214140-53214141 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs547496062 | chr7:53214144-53214145 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs1525574 | chr7:53214203-53214204 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
11 | rs536246656 | chr7:53214234-53214235 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs551768421 | chr7:53214268-53214269 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs111588369 | chr7:53214344-53214345 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs186907411 | chr7:53214353-53214354 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs371769544 | chr7:53214377-53214378 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs547329837 | chr7:53214378-53214379 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs376573027 | chr7:53214401-53214402 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs191697522 | chr7:53214418-53214419 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs1357961 | chr7:53214419-53214420 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
20 | rs75816453 | chr7:53214432-53214433 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs576105156 | chr7:53214448-53214449 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs538329491 | chr7:53214462-53214463 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs112834889 | chr7:53214476-53214477 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs116291182 | chr7:53214496-53214497 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs556684785 | chr7:53214516-53214517 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
26 | rs572102890 | chr7:53214538-53214539 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
27 | rs183492303 | chr7:53214552-53214553 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
28 | rs188334001 | chr7:53214560-53214561 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
29 | rs34157658 | chr7:53214615-53214616 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
30 | rs540642805 | chr7:53214626-53214627 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
31 | rs1357962 | chr7:53214648-53214649 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
32 | rs142333250 | chr7:53214652-53214653 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
33 | rs1357963 | chr7:53214671-53214672 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
34 | rs150011925 | chr7:53214688-53214689 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
35 | rs199848526 | chr7:53214692-53214693 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
36 | rs33969470 | chr7:53214693-53214694 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
37 | rs373371022 | chr7:53214694-53214695 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
38 | rs67791304 | chr7:53214702-53214703 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
39 | rs545082066 | chr7:53214704-53214705 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
40 | rs3054227 | chr7:53214708-53214709 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
41 | rs1357964 | chr7:53214720-53214721 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
42 | rs376046789 | chr7:53214736-53214737 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
43 | rs144099911 | chr7:53214751-53214752 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
44 | rs185466965 | chr7:53214752-53214753 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
45 | rs529101496 | chr7:53214762-53214763 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
46 | rs189588999 | chr7:53214864-53214865 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
47 | rs191277117 | chr7:53214943-53214944 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
48 | rs536109885 | chr7:53214945-53214946 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
49 | rs549973179 | chr7:53215007-53215008 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
50 | rs569777044 | chr7:53215019-53215020 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Glioblastoma multiforme | 17387387 | CNVD |
Astrocytoma | 17387387 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Biliary cancer | 19435499 | CNVD |
Wilms tumour | 21544195 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Glioma | 21971842 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Liposarcoma | 21253554 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Oligodendroglial tumors | 17285580 | CNVD |
Oral cancer | 21386901 | CNVD |
colon cancer | 17210682 | CNVD |
Lung adenocarcinoma | 21810691 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Breast cancer | 21264507 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Hypothalamic hamartomas | 18252217 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Peripheral t-cell lymphoma | 19118030 | CNVD |
Medulloblastoma | 18056178 | CNVD |
Basal cell lymphoma | 17170743 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Seminomas | 18059402 | CNVD |
Testicular cancer | 18059402 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Autism | 19415332 | CNVD |
Pleomorphic xanthoastrocytoma | 20730472 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Malaria | 21533027 | CNVD |
Melanoma | 18172304 | CNVD |
Renal cell carcinoma | 19461508 | CNVD |
head and neck squamous cell carcinoma | 19289630 | CNVD |
Stenocardia | 21860640 | CNVD |
Vasospasm | 21860640 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Lung cancer | 18438408 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Cancer | 21637783 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
Breast cancer | 16397240 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
Glioblastoma multiforme | 17002787 | CNVD |
Autism | 22495311 | CNVD |
Glioblastoma multiforme | 18628472 | CNVD |
Cancer | 21183584 | CNVD |
Breast cancer | 21785460 | CNVD |
Follicular lymphoma | 20505157 | CNVD |
Williams-beuren syndrome | 22470819 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Breast cancer | 21364760 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Multiple myeloma | 16461302 | CNVD |
Glioblastoma multiforme | 21750150 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Gastric cancer | 24379144 | CNVD |
T-cell prolymphocytic leukemia | 17713554 | CNVD |
Pancreatic endocrine tumor | 17639061 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Non-small cell lung cancer | 17643093 | CNVD |
Ovarian cancer | 18182111 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Glioblastoma multiforme | 17369134 | CNVD |
Barrett''s esophagus | 18559552 | CNVD |
head and neck squamous cell carcinoma | 16943533 | CNVD |
Anaplastic thyroid cancer | 17079354 | CNVD |
Basal-like breast cancer | 17875215 | CNVD |
Colorectal cancer | 16882699 | CNVD |
Colorectal cancer | 18794099 | CNVD |
Gastrointestinal stromal cancer | 17643098 | CNVD |
Lung cancer | 18381415 | CNVD |
Metastatic colorectal cancer | 17664472 | CNVD |
Non-small cell lung cancer | 19255323 | CNVD |
Non-small cell lung cancer | 17673923 | CNVD |
Non-small cell lung cancer | 17975165 | CNVD |
Non-small cell lung cancer | 19622585 | CNVD |
Ovarian cancer | 16607561 | CNVD |
Squamous cell cancer | 19670535 | CNVD |
head and neck squamous cell carcinoma | 16818711 | CNVD |
small cell lung cancer | 18829487 | CNVD |
Breast cancer | 17661082 | CNVD |
Adenocarcinoma | 19260752 | CNVD |
Esophageal cancer | 16575012 | CNVD |
Lung adenocarcinoma | 19138956 | CNVD |
Lung adenocarcinoma | 18379350 | CNVD |
Lung adenocarcinoma | 18258923 | CNVD |
Lung cancer | 19138956 | CNVD |
Lung cancer | 18379350 | CNVD |
Lung cancer | 18258923 | CNVD |
Non-small cell lung cancer | 18304967 | CNVD |
Non-small cell lung cancer | 19451690 | CNVD |
Non-small cell lung cancer | 19260752 | CNVD |
Non-small cell lung cancer | 17079354 | CNVD |
Non-small cell lung cancer | 18559607 | CNVD |
Rectal cancer | 19506820 | CNVD |
Triple-negative breast cancer | 18950515 | CNVD |
head and neck squamous cell carcinoma | 18813952 | CNVD |
Non-small cell lung cancer | 17504988 | CNVD |
Non-small cell lung cancer | 16943533 | CNVD |
Non-small cell lung cancer | 18509184 | CNVD |
head and neck squamous cell carcinoma | 17538160 | CNVD |
Colorectal cancer | 19712476 | CNVD |
Lung adenocarcinoma | 19525976 | CNVD |
Lung cancer | 19525976 | CNVD |
Lung cancer | 19671679 | CNVD |
head and neck squamous cell carcinoma | 17671120 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lissencephaly | 21572526 | CNVD |
Breast cancer | 17603634 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Hirschsprung''s Disease | 21712996 | CNVD |
Barrett''s adenocarcinoma | 18663352 | CNVD |
Breast cancer | 21990379 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
Cognitive impairment | 21505072 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
Non-syndromic sensorineural hearing loss | 18451855 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:53214000-53214400 | Enhancers | Brain Germinal Matrix | brain |
2 | chr7:53214000-53215400 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr7:53214200-53214400 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |