Variant report
Variant | esv3433200 |
---|---|
Chromosome Location | chr8:50899999-50904097 |
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 | rs73569374 | chr8:50900013-50900014 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
2 | rs550509534 | chr8:50900027-50900028 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
3 | rs567022478 | chr8:50900036-50900037 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
4 | rs377556493 | chr8:50900083-50900084 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
5 | rs55817447 | chr8:50900089-50900090 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
6 | rs559484108 | chr8:50900112-50900113 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
7 | rs12541852 | chr8:50900135-50900136 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
8 | rs35894770 | chr8:50900138-50900139 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
9 | rs192350525 | chr8:50900144-50900145 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
10 | rs570323303 | chr8:50900165-50900166 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
11 | rs183054198 | chr8:50900171-50900172 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
12 | rs187097866 | chr8:50900191-50900192 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
13 | rs35381511 | chr8:50900209-50900210 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
14 | rs56408284 | chr8:50900226-50900227 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
15 | rs372679497 | chr8:50900231-50900232 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
16 | rs118090516 | chr8:50900269-50900270 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
17 | rs191951260 | chr8:50900270-50900271 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
18 | rs534672686 | chr8:50900278-50900279 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
19 | rs553087559 | chr8:50900285-50900286 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
20 | rs377371662 | chr8:50900301-50900302 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
21 | rs35435708 | chr8:50900317-50900318 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
22 | rs538823080 | chr8:50900338-50900339 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
23 | rs113636127 | chr8:50900353-50900354 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
24 | rs559005669 | chr8:50900354-50900355 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
25 | rs207469141 | chr8:50900358-50900359 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
26 | rs184285233 | chr8:50900366-50900367 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
27 | rs371175879 | chr8:50900392-50900393 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
28 | rs561716857 | chr8:50900402-50900403 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
29 | rs4873401 | chr8:50900416-50900417 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
30 | rs541057073 | chr8:50900443-50900444 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
31 | rs34179442 | chr8:50900444-50900445 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
32 | rs370962068 | chr8:50900446-50900447 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
33 | rs574877572 | chr8:50900513-50900514 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
34 | rs533308258 | chr8:50900561-50900562 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
35 | rs318910 | chr8:50900582-50900583 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
36 | rs77396794 | chr8:50900588-50900589 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
37 | rs531208732 | chr8:50900589-50900590 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
38 | rs318911 | chr8:50900602-50900603 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
39 | rs78171300 | chr8:50900609-50900610 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
40 | rs545153989 | chr8:50900619-50900620 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
41 | rs546664438 | chr8:50900653-50900654 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
42 | rs189052238 | chr8:50900670-50900671 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
43 | rs4242456 | chr8:50900753-50900754 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
44 | rs199937734 | chr8:50900769-50900770 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
45 | rs79556019 | chr8:50900791-50900792 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
46 | rs193251190 | chr8:50900819-50900820 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
47 | rs185717831 | chr8:50900847-50900848 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
48 | rs554425415 | chr8:50900858-50900859 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
49 | rs78495988 | chr8:50900859-50900860 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
50 | rs572850806 | chr8:50900888-50900889 | 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 |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:50898600-50901000 | ZNF genes & repeats | Ganglion Eminence derived primary cultured neurospheres | brain |
2 | chr8:50901000-50901400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |