Variant report
Variant | esv3426268 |
---|---|
Chromosome Location | chr8:51416448-51448918 |
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 | rs139675620 | chr8:51426431-51426432 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
2 | rs532946168 | chr8:51426440-51426441 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
3 | rs184523467 | chr8:51426457-51426458 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
4 | rs189235419 | chr8:51426458-51426459 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
5 | rs545625901 | chr8:51426467-51426468 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
6 | rs539650051 | chr8:51426500-51426501 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
7 | rs377640734 | chr8:51426505-51426506 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
8 | rs549471506 | chr8:51426510-51426511 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
9 | rs117176344 | chr8:51426534-51426535 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
10 | rs377562835 | chr8:51426546-51426547 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
11 | rs576155414 | chr8:51426552-51426553 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
12 | rs181884240 | chr8:51426563-51426564 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
13 | rs145200416 | chr8:51426564-51426565 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
14 | rs574499042 | chr8:51426597-51426598 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
15 | rs541810323 | chr8:51426616-51426617 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
16 | rs560260148 | chr8:51426625-51426626 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
17 | rs527756868 | chr8:51426650-51426651 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
18 | rs552771562 | chr8:51426667-51426668 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
19 | rs528928103 | chr8:51426688-51426689 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
20 | rs530139288 | chr8:51426690-51426691 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
21 | rs564546692 | chr8:51426732-51426733 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
22 | rs2467205 | chr8:51426748-51426749 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
23 | rs186529880 | chr8:51426805-51426806 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
24 | rs78655974 | chr8:51426814-51426815 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
25 | rs568762294 | chr8:51426837-51426838 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
26 | rs535491306 | chr8:51426838-51426839 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
27 | rs375128751 | chr8:51426846-51426847 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
28 | rs547396511 | chr8:51426866-51426867 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
29 | rs565817835 | chr8:51426877-51426878 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
30 | rs57988555 | chr8:51426899-51426900 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
31 | rs576667292 | chr8:51426931-51426932 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
32 | rs62515747 | chr8:51426939-51426940 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
33 | rs371436413 | chr8:51426954-51426955 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
34 | rs576158851 | chr8:51426962-51426963 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
35 | rs537207919 | chr8:51426996-51426997 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
36 | rs4873462 | chr8:51427070-51427071 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
37 | rs555280343 | chr8:51427088-51427089 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
38 | rs192040621 | chr8:51427139-51427140 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
39 | rs374574599 | chr8:51427142-51427143 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
40 | rs367583574 | chr8:51427149-51427150 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
41 | rs118073411 | chr8:51427193-51427194 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
42 | rs560098845 | chr8:51427197-51427198 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
43 | rs180748254 | chr8:51427199-51427200 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
44 | rs183159063 | chr8:51428408-51428409 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
45 | rs533657481 | chr8:51428432-51428433 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
46 | rs117361706 | chr8:51428433-51428434 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
47 | rs563312458 | chr8:51428434-51428435 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
48 | rs530397499 | chr8:51428448-51428449 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
49 | rs540304526 | chr8:51428452-51428453 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
50 | rs188939708 | chr8:51428453-51428454 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Cancer | 16751803 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Wilms tumour | 21544195 | CNVD |
Gastric cancer | 17908304 | CNVD |
Melanoma | 18172304 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Autism | 19415332 | CNVD |
Malaria | 21533027 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Breast cancer | 21245420 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Seminomas | 18059402 | CNVD |
Autism | 22495311 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Pancreatic cancer | 21811587 | CNVD |
Multiple myeloma | 16461302 | CNVD |
Developmental delay | 21373258 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Breast cancer | 17603634 | CNVD |
Pancreatic endocrine tumor | 17639061 | CNVD |
Disorders of sex development | 21048976 | CNVD |
Testicular cancer | 18059402 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Salivary gland tumor | 18059337 | CNVD |
Breast cancer | 17133270 | CNVD |
Breast cancer | 21509527 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Breast cancer | 21858162 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Acute lymphoblastic leukemia | 21248843 | CNVD |
Cancer | 20164919 | CNVD |
primary effusion lymphomas | 17116491 | CNVD |
Esophageal cancer | 20955586 | CNVD |
abnormal development | 18461090 | CNVD |
Cancer | 20164920 | CNVD |
low-grade B-cell lymphoma tumor | 18367492 | CNVD |
Oral cancer | 21386901 | CNVD |
Uveal melanoma | 21693616 | CNVD |
Langer-Giedion syndrome | 22283845 | CNVD |
Cancer | 21637783 | CNVD |
Splenic marginal zone lymphoma | 21957467 | CNVD |
Breast cancer | 20632083 | CNVD |
Breast cancer | 19602461 | CNVD |
Cancer | 22429812 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Oral cancer | 19627613 | CNVD |
Prostate cancer | 21088497 | CNVD |
colon cancer | 17210682 | CNVD |
Breast cancer | 21264507 | CNVD |
Breast cancer | 22028636 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Gastric cancer | 17167181 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Breast cancer | 16461572 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Medulloblastoma | 16968546 | CNVD |
head and neck squamous cell carcinoma | 18028549 | CNVD |
Breast cancer | 17001317 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lung cancer | 18438408 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Prostate cancer | 16461572 | CNVD |
Breast cancer | 16608533 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Melanoma | 17363583 | CNVD |
Prostate cancer | 18632612 | CNVD |
Glioblastoma multiforme | 18628472 | CNVD |
Sezary syndrome | 18413736 | CNVD |
Ovarian cancer | 22174824 | CNVD |
Pancreatic ductal adenocarcinoma | 19077451 | CNVD |
22q11 deletion syndrome | 20357662 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:51426400-51427200 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
2 | chr8:51428400-51429800 | ZNF genes & repeats | Ganglion Eminence derived primary cultured neurospheres | brain |
3 | chr8:51441000-51469200 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
4 | chr8:51444200-51444400 | Enhancers | Gastric | stomach |