Variant report
Variant | esv3443872 |
---|---|
Chromosome Location | chr5:68260446-68262944 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:18)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:18 , 50 per page) page:
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No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | BCL3 | chr5:68260303-68262196 | GM12878 | blood: | n/a | n/a |
2 | BCL3 | chr5:68260450-68262189 | GM12878 | blood: | n/a | n/a |
3 | CTCF | chr5:68261862-68261988 | GM19239 | blood: | n/a | n/a |
4 | CTCF | chr5:68261771-68261782 | GM13976 | blood: | n/a | n/a |
5 | CTCF | chr5:68261080-68261230 | HCFaa | heart: | n/a | n/a |
6 | CTCF | chr5:68260697-68260754 | GM19239 | blood: | n/a | n/a |
7 | NFATC1 | chr5:68260454-68261635 | GM12878 | blood: | n/a | n/a |
8 | NFATC1 | chr5:68261608-68262132 | GM12878 | blood: | n/a | n/a |
9 | NFATC1 | chr5:68260253-68261422 | GM12878 | blood: | n/a | n/a |
10 | NFATC1 | chr5:68261711-68262150 | GM12878 | blood: | n/a | n/a |
11 | NR2C2 | chr5:68260475-68261442 | GM12878 | blood: | n/a | n/a |
12 | PBX3 | chr5:68260971-68261252 | GM12878 | blood: | n/a | n/a |
13 | PBX3 | chr5:68261287-68262073 | GM12878 | blood: | n/a | n/a |
14 | PBX3 | chr5:68260495-68260905 | GM12878 | blood: | n/a | n/a |
15 | POLR2A | chr5:68261821-68261826 | Gliobla | brain: | n/a | n/a |
16 | POLR2A | chr5:68261772-68261775 | Gliobla | brain: | n/a | n/a |
17 | RCOR1 | chr5:68260691-68260805 | K562 | blood: | n/a | n/a |
18 | SUZ12 | chr5:68260542-68261541 | H1-hESC | embryonic stem cell: | n/a | n/a |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr5:68258016..68260416-chr5:68261824..68264961,3 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000249335 | TF binding region |
ENSG00000250066 | chromatin interactions |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs528674783 | chr5:68260463-68260464 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
2 | rs553652827 | chr5:68260481-68260482 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
3 | rs565877866 | chr5:68260482-68260483 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
4 | rs539100816 | chr5:68260556-68260557 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
5 | rs114455375 | chr5:68260564-68260565 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
6 | rs200691999 | chr5:68260568-68260569 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
7 | rs558784163 | chr5:68260572-68260573 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
8 | rs575623525 | chr5:68260577-68260578 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
9 | rs534485797 | chr5:68260584-68260585 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
10 | rs373965310 | chr5:68260589-68260590 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
11 | rs543042204 | chr5:68260591-68260592 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
12 | rs111842415 | chr5:68260598-68260599 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
13 | rs555362965 | chr5:68260599-68260600 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
14 | rs374330910 | chr5:68260600-68260601 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
15 | rs9800367 | chr5:68260616-68260617 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | LD-proxies of rSNPOverlapped rCNV | n/a |
16 | rs543158251 | chr5:68260630-68260631 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
17 | rs57150368 | chr5:68260652-68260653 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | LD-proxies of rSNPOverlapped rCNV | n/a |
18 | rs56994272 | chr5:68260666-68260667 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | LD-proxies of rSNPOverlapped rCNV | n/a |
19 | rs369287647 | chr5:68260686-68260687 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
20 | rs563809779 | chr5:68260691-68260692 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
21 | rs576731813 | chr5:68260692-68260693 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
22 | rs548457313 | chr5:68260696-68260697 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
23 | rs530908294 | chr5:68260707-68260708 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
24 | rs186214130 | chr5:68260708-68260709 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
25 | rs567669092 | chr5:68260722-68260723 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
26 | rs191506238 | chr5:68260734-68260735 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
27 | rs565545142 | chr5:68260735-68260736 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
28 | rs182774187 | chr5:68260737-68260738 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
29 | rs367873479 | chr5:68260759-68260760 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
30 | rs551039473 | chr5:68260760-68260761 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
31 | rs558403961 | chr5:68260767-68260768 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
32 | rs569382899 | chr5:68260771-68260772 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
33 | rs376837703 | chr5:68260793-68260794 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
34 | rs530322835 | chr5:68260795-68260796 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
35 | rs570069186 | chr5:68260796-68260797 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
36 | rs536763760 | chr5:68260800-68260801 | ZNF genes & repeats Weak transcription Enhancers | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
37 | rs555020691 | chr5:68260801-68260802 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
38 | rs573582752 | chr5:68260815-68260816 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
39 | rs369215254 | chr5:68260833-68260834 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
40 | rs138878558 | chr5:68260845-68260846 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
41 | rs139123353 | chr5:68260846-68260847 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
42 | rs140426999 | chr5:68260847-68260848 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
43 | rs151118830 | chr5:68260848-68260849 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
44 | rs563896653 | chr5:68260852-68260853 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
45 | rs552320417 | chr5:68260859-68260860 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
46 | rs575776767 | chr5:68260861-68260862 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
47 | rs567866135 | chr5:68260869-68260870 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
48 | rs145249979 | chr5:68260871-68260872 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
49 | rs111066623 | chr5:68260887-68260888 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
50 | rs556983694 | chr5:68260897-68260898 | ZNF genes & repeats Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
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 |
Colorectal cancer | 21645411 | CNVD |
Gastric cancer | 22152101 | CNVD |
Oesophago-gastric ulcer | 22152101 | CNVD |
Ovarian cancer | 21781307 | CNVD |
Breast cancer | 20668451 | CNVD |
Cancer | 20668451 | CNVD |
Lung cancer | 20668451 | CNVD |
Ovarian cancer | 20668451 | CNVD |
Pancreas cancer | 20668451 | CNVD |
Prostate cancer | 20668451 | CNVD |
Cancer | 20164919 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
DNA damage stimulus | 22844521 | CNVD |
DNA repair | 22844521 | CNVD |
Breast cancer | 21785460 | CNVD |
Spinal muscular atrophy | 22422766 | CNVD |
Spinal muscular atrophy | 22558076 | CNVD |
Spinal muscular atrophy | 21320981 | CNVD |
Spinal muscular atrophy | 21762474 | CNVD |
Cancer | 16751803 | CNVD |
Intellectual disability | 22102821 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Breast cancer | 17603634 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Melanoma | 18172304 | CNVD |
Glioma | 20126413 | CNVD |
Breast cancer | 22032731 | CNVD |
Prostate cancer | 21965145 | CNVD |
Esophageal cancer | 20955586 | CNVD |
Congenital anomalies of the kidney and urinary tract | 18694510 | CNVD |
Ovarian cancer | 20844748 | CNVD |
Breast cancer | 17393978 | CNVD |
Cancer | 21359685 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
adenomatous polyposis | 22470819 | 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 |
Hepatocellular carcinoma | 16750200 | 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 |
Acute myeloid leukemia | 20729466 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Oral cancer | 21386901 | CNVD |
Bladder cancer | 21909424 | CNVD |
Esophageal adenocarcinoma | 19417022 | CNVD |
Barrett''s syndrome | 19417022 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lung cancer | 18438408 | CNVD |
Breast cancer | 17133270 | CNVD |
Breast cancer | 19602461 | CNVD |
Esophageal adenocarcinoma | 18519675 | CNVD |
Retinoblastoma | 22278416 | CNVD |
Bipolar disorder | 18458673 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
abnormal development | 18461090 | CNVD |
Esophageal squamous carcinoma | 18405350 | CNVD |
Merkel cell carcinoma | 19020549 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
Neurodevelopmental disorder | 22521361 | CNVD |
Prostate cancer | 18632612 | CNVD |
Ovarian cancer | 21720365 | CNVD |
Lung adenocarcinoma | 17086460 | CNVD |
Breast cancer | 21045282 | CNVD |
Chronic lymphocytic leukemia | 18922857 | CNVD |
Lung cancer | 17086460 | CNVD |
Prostate cancer | 16461572 | CNVD |
Myelodysplastic syndrome | 18663149 | CNVD |
Spinal muscular atrophy | 15981080 | CNVD |
Spinal muscular atrophy | 18839960 | CNVD |
Spinal muscular atrophy | 19716110 | CNVD |
Sezary syndrome | 18413736 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:68246200-68262200 | Weak transcription | Esophagus | oesophagus |
2 | chr5:68258000-68261800 | Weak transcription | Spleen | Spleen |
3 | chr5:68258800-68262000 | Weak transcription | Brain Substantia Nigra | brain |
4 | chr5:68258800-68262000 | Weak transcription | Fetal Muscle Trunk | muscle |
5 | chr5:68259200-68262200 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
6 | chr5:68260400-68260600 | Enhancers | Fetal Lung | lung |
7 | chr5:68260400-68260800 | Enhancers | Gastric | stomach |
8 | chr5:68260400-68260800 | Enhancers | Pancreas | Pancrea |
9 | chr5:68260400-68261400 | ZNF genes & repeats | H9 Cell Line | embryonic stem cell |
10 | chr5:68260400-68261600 | ZNF genes & repeats | Fetal Kidney | kidney |
11 | chr5:68260600-68260800 | ZNF genes & repeats | Fetal Lung | lung |
12 | chr5:68260600-68261400 | ZNF genes & repeats | Fetal Brain Male | brain |
13 | chr5:68261400-68262400 | Weak transcription | Fetal Brain Male | brain |
14 | chr5:68261800-68262000 | Enhancers | Spleen | Spleen |
15 | chr5:68262000-68262600 | Enhancers | Fetal Muscle Trunk | muscle |
16 | chr5:68262200-68262600 | Enhancers | Breast Myoepithelial Primary Cells | Breast |