Variant report
Variant | nsv892811 |
---|---|
Chromosome Location | chr9:25098890-25176251 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr9:25096345..25098093-chr9:25100107..25101850,2 | MCF-7 | breast: | |
2 | chr9:25175084..25177209-chr9:25178097..25179794,2 | MCF-7 | breast: | |
3 | chr9:25135319..25136895-chr9:25139782..25142029,2 | MCF-7 | breast: | |
4 | chr9:25135319..25136895-chr9:25139782..25142029,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs116109955 | chr9:25115011-25115012 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs79856425 | chr9:25115031-25115032 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs551059176 | chr9:25115036-25115037 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs571174466 | chr9:25115089-25115090 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs144613655 | chr9:25115113-25115114 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs547217988 | chr9:25115120-25115121 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs181907098 | chr9:25115150-25115151 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs147887155 | chr9:25115151-25115152 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs3118252 | chr9:25115154-25115155 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
10 | rs569230970 | chr9:25115156-25115157 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs538262089 | chr9:25115163-25115164 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs557697984 | chr9:25115243-25115244 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs577528080 | chr9:25115247-25115248 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs540091427 | chr9:25115251-25115252 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs553650929 | chr9:25115282-25115283 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs78887367 | chr9:25115319-25115320 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs75740466 | chr9:25115325-25115326 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs148015110 | chr9:25115352-25115353 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs112071333 | chr9:25115367-25115368 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs186556386 | chr9:25115400-25115401 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs568663878 | chr9:25115414-25115415 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs139387722 | chr9:25115459-25115460 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs150061846 | chr9:25115498-25115499 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs527274186 | chr9:25115501-25115502 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs76976218 | chr9:25115513-25115514 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
26 | rs189770087 | chr9:25115519-25115520 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
27 | rs529519622 | chr9:25115545-25115546 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
28 | rs182949234 | chr9:25115554-25115555 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
29 | rs28698306 | chr9:25115558-25115559 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
30 | rs537914092 | chr9:25115559-25115560 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
31 | rs557735139 | chr9:25115597-25115598 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
32 | rs561923663 | chr9:25115608-25115609 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs528417222 | chr9:25115630-25115631 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs186222200 | chr9:25115681-25115682 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs145317884 | chr9:25115697-25115698 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs572529197 | chr9:25115700-25115701 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs117628942 | chr9:25115703-25115704 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
38 | rs536459537 | chr9:25115754-25115755 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
39 | rs556043407 | chr9:25115764-25115765 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs576088609 | chr9:25115765-25115766 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs544822508 | chr9:25115796-25115797 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs149195690 | chr9:25115797-25115798 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
43 | rs145126971 | chr9:25115808-25115809 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
44 | rs146446843 | chr9:25115821-25115822 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs560788860 | chr9:25115822-25115823 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs529527822 | chr9:25115826-25115827 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
47 | rs528953481 | chr9:25115860-25115861 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
48 | rs373085391 | chr9:25115882-25115883 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
49 | rs562895248 | chr9:25115883-25115884 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
50 | rs531931206 | chr9:25115885-25115886 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Glioblastoma multiforme | 21080181 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Breast cancer | 16608533 | CNVD |
Hodgkin''s lymphoma | 18641027 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Breast cancer | 16272173 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Breast cancer | 17133270 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Cervical cancer | 21063398 | CNVD |
Retinoblastoma | 22278416 | CNVD |
Splenic marginal zone lymphoma | 18492102 | CNVD |
Melanoma | 18172304 | CNVD |
Biliary cancer | 19435499 | CNVD |
Gastric cancer | 21586687 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Myopathy | 18421352 | CNVD |
Neuroblastoma | 18664255 | CNVD |
Acute lymphoblastic leukemia | 18957548 | CNVD |
Myeloproliferative neoplasm | 17564968 | CNVD |
Malignant meningioma | 17937814 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Glioma | 21971842 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 17603634 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Breast cancer | 21264507 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Oligodendroglial tumors | 17285580 | CNVD |
Cutaneous squamous cell carcinomas | 19131950 | CNVD |
Small bowel adenocarcinoma | 21586687 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Chordoma | 18071362 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Chordoma | 21602918 | CNVD |
Renal cell carcinoma | 18592004 | CNVD |
Developmental delay | 19490664 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Pleomorphic xanthoastrocytoma | 20730472 | CNVD |
microdeletion syndrome | 16199537 | CNVD |
Non-syndromic sensorineural hearing loss | 21987784 | CNVD |
Cancer | 20164919 | CNVD |
Ovarian cancer | 21720365 | CNVD |
Non-syndromic sensorineural hearing loss | 21030649 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Lung cancer | 18438408 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Acute lymphoblastic leukemia | 21339820 | CNVD |
Chronic myeloid leukemia | 21384125 | CNVD |
Breast cancer | 21785460 | CNVD |
Esophageal adenocarcinoma | 19417022 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Renal cell carcinoma | 21668985 | CNVD |
Myelodysplastic syndrome | 21251322 | CNVD |
Autism | 22495311 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Developmental delay | 21147756 | CNVD |
Pilocytic astrocytoma | 18670637 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Melanoma | 22183965 | CNVD |
Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
Non-small cell lung cancer | 19010865 | CNVD |
Myoepithelioma | 18604193 | CNVD |
Cancer | 22183965 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Ewing''s sarcoma | 22429812 | CNVD |
Neuroblastoma | 21899760 | CNVD |
Glioblastoma multiforme | 19435819 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Cutaneous T-cell lymphoma | 21881587 | CNVD |
Glioblastoma multiforme | 22291905 | CNVD |
Lung cancer | 21911935 | CNVD |
Primary central nervous system lymphoma | 21088137 | CNVD |
head and neck squamous cell carcinoma | 21798897 | CNVD |
Cancer | 21253487 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Intracranial ependymoma | 16609018 | CNVD |
Gastrointestinal stromal cancer | 16982739 | CNVD |
Glioblastoma multiforme | 21922591 | CNVD |
Acute lymphoblastic leukemia | 17443227 | CNVD |
Barrett''s adenocarcinoma | 18663352 | CNVD |
T-cell acute lymphoblastic leukemia | 19406988 | CNVD |
Urothelial cell carcinoma | 18451213 | CNVD |
Glioma | 17123091 | CNVD |
Mental retardation | 17124404 | CNVD |
Acute lymphoblastic leukemia | 19100363 | CNVD |
Acute lymphoblastic leukemia | 18768390 | CNVD |
Leukemia | 19602459 | CNVD |
Acute monocytic leukemia | 16498392 | CNVD |
Esophageal squamous carcinoma | 18405350 | CNVD |
Malignant mesothelioma | 18160781 | CNVD |
Pleural malignant mesothelioma | 18160781 | CNVD |
Leukemia | 18688285 | CNVD |
T-cell acute lymphoblastic leukemia | 18185524 | CNVD |
Acute myeloid leukemia | 19651601 | CNVD |
Coronary Disease | 20032323 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
Hirschsprung''s Disease | 21712996 | CNVD |
Cancer | 21732550 | CNVD |
Gastric cancer | 22539939 | CNVD |
Cancer | 21183584 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Diffuse large b-cell lymphoma | 18287131 | CNVD |
Metastatic melanoma | 18483359 | CNVD |
Non-small cell lung cancer | 20864512 | CNVD |
Cervical cancer | 21062161 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Glioblastoma | 17090523 | CNVD |
Lung cancer | 16773561 | CNVD |
Adenoid cystic carcinoma | 17372589 | CNVD |
Colorectal cancer | 16774939 | CNVD |
Bladder cancer | 19088036 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Melanoma | 16977458 | CNVD |
Glioblastoma multiforme | 17369134 | CNVD |
Chagasic megaesophagus | 20163722 | CNVD |
Melanoma | 19566914 | CNVD |
Squamous cell cancer | 19047905 | CNVD |
Lung adenocarcinoma | 19525976 | CNVD |
Lung cancer | 19525976 | CNVD |
Hodgkin''s lymphoma | 18179710 | CNVD |
Melanoma | 17363583 | CNVD |
Adenoid cystic carcinoma | 18332873 | CNVD |
low-grade B-cell lymphoma tumor | 18367492 | CNVD |
Ovarian clear cell carcinoma | 21343371 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Oral cancer | 21386901 | CNVD |
Breast cancer | 21858162 | CNVD |
Breast cancer | 21364760 | CNVD |
Esophageal adenocarcinoma | 18519675 | CNVD |
Lung cancer | 21569311 | CNVD |
Pancreatic cancer | 21811587 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:25115000-25115600 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
2 | chr9:25115600-25117400 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
3 | chr9:25117400-25118000 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
4 | chr9:25118000-25119600 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
5 | chr9:25118400-25120200 | Enhancers | Fetal Lung | lung |
6 | chr9:25119600-25120000 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |