Variant report
Variant | esv3427099 |
---|---|
Chromosome Location | chr5:124233328-124236251 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-ZNF608-15 | chr5:124232481-124233502 | l_3006_chr5:124232480-124239722_testes |
No data |
No data |
No data |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs534568983 | chr5:124233352-124233353 | Weak transcription ZNF genes & repeats Enhancers | lncRNA | n/a | Overlapped CNVs | n/a |
2 | rs553316542 | chr5:124233371-124233372 | Weak transcription ZNF genes & repeats Enhancers | lncRNA | n/a | Overlapped CNVs | n/a |
3 | rs189998203 | chr5:124233386-124233387 | Weak transcription ZNF genes & repeats Enhancers | lncRNA | n/a | Overlapped CNVs | n/a |
4 | rs538924130 | chr5:124233407-124233408 | ZNF genes & repeats Weak transcription | lncRNA | n/a | Overlapped CNVs | n/a |
5 | rs556918953 | chr5:124233455-124233456 | ZNF genes & repeats Weak transcription | lncRNA | n/a | Overlapped CNVs | n/a |
6 | rs575383218 | chr5:124233516-124233517 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs543540250 | chr5:124233528-124233529 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs561819266 | chr5:124233537-124233538 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs543873014 | chr5:124233549-124233550 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs181264477 | chr5:124233581-124233582 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs140217289 | chr5:124233629-124233630 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs563635591 | chr5:124233671-124233672 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs559997421 | chr5:124233687-124233688 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs77028759 | chr5:124233696-124233697 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs537994061 | chr5:124233726-124233727 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs184340718 | chr5:124233781-124233782 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs6864634 | chr5:124233789-124233790 | ZNF genes & repeats Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
18 | rs75187406 | chr5:124233833-124233834 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
19 | rs149726901 | chr5:124233855-124233856 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
20 | rs188780518 | chr5:124233867-124233868 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
21 | rs566126108 | chr5:124233946-124233947 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs199554075 | chr5:124234034-124234035 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
23 | rs549310154 | chr5:124234039-124234040 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
24 | rs567619223 | chr5:124234057-124234058 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
25 | rs34921712 | chr5:124234067-124234068 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs181920586 | chr5:124234070-124234071 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs538080229 | chr5:124234071-124234072 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs113820104 | chr5:124234082-124234083 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs549948093 | chr5:124234116-124234117 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs571271905 | chr5:124234143-124234144 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs538700211 | chr5:124234168-124234169 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs371646737 | chr5:124234170-124234171 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs186385103 | chr5:124234179-124234180 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs571966469 | chr5:124234244-124234245 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs536244412 | chr5:124234447-124234448 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs377568572 | chr5:124234491-124234492 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs370472480 | chr5:124234492-124234493 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
38 | rs567332666 | chr5:124234512-124234513 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
39 | rs554949082 | chr5:124234547-124234548 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs576381610 | chr5:124234566-124234567 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs534606850 | chr5:124234574-124234575 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs543674486 | chr5:124234578-124234579 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
43 | rs565037092 | chr5:124234580-124234581 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
44 | rs546668644 | chr5:124234588-124234589 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs578048527 | chr5:124234610-124234611 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs376241121 | chr5:124234621-124234622 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
47 | rs545434685 | chr5:124234642-124234643 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
48 | rs560292872 | chr5:124234644-124234645 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
49 | rs527735505 | chr5:124234651-124234652 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
50 | rs548946351 | chr5:124234660-124234661 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Metanephric adenoma | 20802469 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Gastrointestinal stromal cancer | 16982739 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Phyllodes tumor | 17334353 | CNVD |
Malaria | 21533027 | CNVD |
Renal cell carcinoma | 19461508 | CNVD |
Cancer | 20164919 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Cancer | 16751803 | CNVD |
Intellectual disability | 22102821 | CNVD |
Breast cancer | 17603634 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Melanoma | 18172304 | CNVD |
Glioma | 20126413 | CNVD |
Cancer | 22429812 | CNVD |
Cancer | 21637783 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
Liposarcoma | 21253554 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Breast cancer | 21264507 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Breast cancer | 21858162 | CNVD |
Leukemia | 17361228 | CNVD |
Myelodysplastic syndrome | 18508791 | CNVD |
5q-syndrome | 17576883 | CNVD |
Gastric cancer | 17908304 | CNVD |
Lung cancer | 16740712 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Esophageal adenocarcinoma | 19417022 | CNVD |
Barrett''s syndrome | 19417022 | CNVD |
Lung cancer | 18438408 | CNVD |
Bipolar disorder | 18458673 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Breast cancer | 21785460 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Neurodevelopmental disorder | 22521361 | CNVD |
Prostate cancer | 18632612 | CNVD |
Breast cancer | 17133270 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Cancer | 20164920 | CNVD |
Myelodysplastic syndrome | 21251322 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Hodgkin''s lymphoma | 18641027 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Ovarian cancer | 21720365 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Salivary gland tumor | 18059337 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Renal cell carcinoma | 19377443 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Gastrointestinal stromal cancer | 19259404 | CNVD |
Renal cell carcinoma | 18194544 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Breast cancer | 16397240 | CNVD |
Parathyroid adenoma | 22454399 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Malignant fibrous histiocytomas | 21085701 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:124223200-124242200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr5:124225800-124237800 | Weak transcription | Fetal Lung | lung |
3 | chr5:124233000-124233400 | ZNF genes & repeats | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
4 | chr5:124233000-124233400 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
5 | chr5:124233000-124233800 | ZNF genes & repeats | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
6 | chr5:124233200-124233400 | ZNF genes & repeats | H9 Cell Line | embryonic stem cell |
7 | chr5:124233200-124233400 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
8 | chr5:124233400-124234000 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
9 | chr5:124233400-124237600 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
10 | chr5:124233800-124234200 | Weak transcription | H9 Cell Line | embryonic stem cell |
11 | chr5:124233800-124238000 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
12 | chr5:124234000-124236000 | Weak transcription | H1 Cell Line | embryonic stem cell |
13 | chr5:124235200-124242000 | Weak transcription | NHDF-Ad | bronchial |