Variant report
Variant | nsv607086 |
---|---|
Chromosome Location | chr7:57638100-57639830 |
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 | rs140737904 | chr7:57639202-57639203 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
2 | rs189350322 | chr7:57639203-57639204 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
3 | rs138547145 | chr7:57639206-57639207 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
4 | rs181763478 | chr7:57639208-57639209 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
5 | rs116536131 | chr7:57639244-57639245 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
6 | rs75814532 | chr7:57639251-57639252 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
7 | rs562717112 | chr7:57639253-57639254 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
8 | rs574697182 | chr7:57639285-57639286 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
9 | rs541485971 | chr7:57639289-57639290 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
10 | rs73701840 | chr7:57639293-57639294 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
11 | rs548099711 | chr7:57639294-57639295 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
12 | rs112306445 | chr7:57639300-57639301 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
13 | rs372915816 | chr7:57639302-57639303 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
14 | rs563940316 | chr7:57639305-57639306 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
15 | rs568228462 | chr7:57639308-57639309 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
16 | rs200138557 | chr7:57639336-57639337 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
17 | rs531605040 | chr7:57639352-57639353 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
18 | rs550101638 | chr7:57639361-57639362 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
19 | rs568218792 | chr7:57639370-57639371 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
20 | rs73129291 | chr7:57639371-57639372 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
21 | rs7810986 | chr7:57639373-57639374 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
22 | rs548695576 | chr7:57639380-57639381 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
23 | rs185162617 | chr7:57639388-57639389 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
24 | rs533928831 | chr7:57639389-57639390 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
25 | rs558880080 | chr7:57639399-57639400 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
26 | rs374103132 | chr7:57639408-57639409 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
27 | rs367997708 | chr7:57639411-57639412 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
28 | rs374435166 | chr7:57639412-57639413 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
29 | rs556450287 | chr7:57639413-57639414 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
30 | rs574684684 | chr7:57639414-57639415 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
31 | rs542065722 | chr7:57639415-57639416 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
32 | rs530943380 | chr7:57639416-57639417 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
33 | rs374185234 | chr7:57639423-57639424 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
34 | rs145146944 | chr7:57639440-57639441 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
35 | rs572217849 | chr7:57639443-57639444 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
36 | rs188063540 | chr7:57639446-57639447 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
37 | rs564063000 | chr7:57639452-57639453 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
38 | rs200281767 | chr7:57639455-57639456 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
39 | rs146872247 | chr7:57639472-57639473 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
40 | rs550088055 | chr7:57639487-57639488 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
41 | rs377058444 | chr7:57639494-57639495 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
42 | rs562007145 | chr7:57639526-57639527 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
43 | rs77199930 | chr7:57639536-57639537 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
44 | rs202163521 | chr7:57639596-57639597 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
45 | rs73701841 | chr7:57639605-57639606 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
46 | rs79181583 | chr7:57639608-57639609 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
47 | rs79812735 | chr7:57639623-57639624 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
48 | rs547644147 | chr7:57639648-57639649 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
49 | rs181413194 | chr7:57639665-57639666 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
50 | rs76532686 | chr7:57639674-57639675 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
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 |
Esophageal squamous carcinoma | 21637470 | 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 |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Autism | 22495311 | CNVD |
Biliary cancer | 19435499 | CNVD |
Cancer | 21183584 | CNVD |
Follicular lymphoma | 20505157 | CNVD |
Williams-beuren syndrome | 22470819 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Multiple myeloma | 16461302 | CNVD |
Glioblastoma multiforme | 21750150 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
Gastric cancer | 24379144 | CNVD |
Glioblastoma multiforme | 17002787 | CNVD |
Lung cancer | 18438408 | CNVD |
T-cell prolymphocytic leukemia | 17713554 | CNVD |
head and neck squamous cell carcinoma | 17671120 | CNVD |
Lissencephaly | 21572526 | CNVD |
Breast cancer | 17603634 | CNVD |
Breast cancer | 16397240 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Glioma | 17634744 | CNVD |
Oral squamous cell carcinoma | 19276369 | CNVD |
Ovine squamous-cell carcinoma | 17599052 | CNVD |
Lung cancer | 20031968 | CNVD |
Glioblastoma | 17090523 | CNVD |
Esophageal squamous carcinoma | 18405350 | CNVD |
Glioma | 17123091 | CNVD |
Hodgkin''s lymphoma | 18641027 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Breast cancer | 21364760 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Schizophrenia | 21399695 | CNVD |
Schizophrenia | 20967226 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:57639200-57641400 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |