Variant report
Variant | nsv508536 |
---|---|
Chromosome Location | chr9:15811619-15834267 |
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 | rs556988847 | chr9:15811632-15811633 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
2 | rs575243164 | chr9:15811685-15811686 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
3 | rs150285584 | chr9:15811691-15811692 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
4 | rs564500001 | chr9:15811739-15811740 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
5 | rs115221154 | chr9:15811745-15811746 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
6 | rs540902881 | chr9:15811807-15811808 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
7 | rs562161412 | chr9:15811814-15811815 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
8 | rs529484645 | chr9:15811850-15811851 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
9 | rs548312167 | chr9:15811857-15811858 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
10 | rs563335390 | chr9:15811888-15811889 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
11 | rs74327770 | chr9:15811930-15811931 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
12 | rs573307600 | chr9:15811934-15811935 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
13 | rs570407638 | chr9:15811952-15811953 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
14 | rs373644072 | chr9:15811964-15811965 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
15 | rs7849380 | chr9:15811980-15811981 | Weak transcription ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
16 | rs12002511 | chr9:15811988-15811989 | Weak transcription ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
17 | rs567915890 | chr9:15811993-15811994 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
18 | rs137971537 | chr9:15812019-15812020 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
19 | rs12001109 | chr9:15812026-15812027 | Weak transcription ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
20 | rs564330360 | chr9:15812037-15812038 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
21 | rs564948680 | chr9:15812041-15812042 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
22 | rs575378267 | chr9:15812045-15812046 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
23 | rs142448939 | chr9:15812071-15812072 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
24 | rs557899015 | chr9:15812077-15812078 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
25 | rs573154631 | chr9:15812111-15812112 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
26 | rs540593928 | chr9:15812135-15812136 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
27 | rs562325201 | chr9:15812140-15812141 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
28 | rs574296872 | chr9:15812141-15812142 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
29 | rs58633569 | chr9:15812162-15812163 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
30 | rs57078810 | chr9:15812164-15812165 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
31 | rs371685963 | chr9:15812197-15812198 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
32 | rs544860859 | chr9:15812211-15812212 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
33 | rs563069862 | chr9:15812223-15812224 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
34 | rs59106947 | chr9:15812239-15812240 | Weak transcription ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
35 | rs552235441 | chr9:15812264-15812265 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
36 | rs116097623 | chr9:15812283-15812284 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
37 | rs528039906 | chr9:15812286-15812287 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
38 | rs546587443 | chr9:15812294-15812295 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
39 | rs146375314 | chr9:15812307-15812308 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
40 | rs535356184 | chr9:15812370-15812371 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
41 | rs7866641 | chr9:15812396-15812397 | Weak transcription ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
42 | rs111472375 | chr9:15812405-15812406 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
43 | rs560931252 | chr9:15812408-15812409 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
44 | rs73420322 | chr9:15812416-15812417 | Weak transcription ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
45 | rs558206438 | chr9:15812453-15812454 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
46 | rs573161934 | chr9:15812480-15812481 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
47 | rs561266142 | chr9:15812495-15812496 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
48 | rs77022308 | chr9:15812524-15812525 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
49 | rs78752420 | chr9:15812553-15812554 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
50 | rs544898900 | chr9:15812560-15812561 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Chronic lymphocytic leukemia | 21546498 | CNVD |
abnormal development | 18461090 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
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 |
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 |
Pleomorphic xanthoastrocytoma | 20730472 | CNVD |
microdeletion syndrome | 16199537 | CNVD |
Non-syndromic sensorineural hearing loss | 21987784 | CNVD |
Cancer | 20164919 | CNVD |
Chronic myeloid leukemia | 21384125 | 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 |
Oral cancer | 21386901 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Acute lymphoblastic leukemia | 21339820 | CNVD |
Intellectual disability | 22102821 | CNVD |
Breast cancer | 21785460 | CNVD |
Esophageal adenocarcinoma | 19417022 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Breast cancer | 21858162 | CNVD |
Renal cell carcinoma | 21668985 | CNVD |
Myelodysplastic syndrome | 21251322 | CNVD |
Autism | 22495311 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Breast cancer | 21364760 | CNVD |
Prostate cancer | 16573809 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Developmental delay | 21147756 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Pilocytic astrocytoma | 18670637 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Melanoma | 22183965 | CNVD |
low-grade B-cell lymphoma tumor | 18367492 | CNVD |
Breast cancer | 21611746 | CNVD |
Glycine encephalopathy | 21572526 | CNVD |
Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
Non-small cell lung cancer | 19010865 | CNVD |
Myoepithelioma | 18604193 | CNVD |
Glioblastoma multiforme | 18628472 | CNVD |
Ovarian cancer | 19835627 | CNVD |
Breast cancer | 22522925 | CNVD |
Autism | 20858261 | CNVD |
Epilepsy | 20858261 | CNVD |
Mental retardation | 20858261 | CNVD |
Pancreatic ductal adenocarcinoma | 19077451 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:15805600-15812600 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
2 | chr9:15811200-15815000 | Weak transcription | Primary hematopoietic stem cells | blood |
3 | chr9:15811200-15816000 | Weak transcription | Pancreas | Pancrea |
4 | chr9:15812000-15813400 | Weak transcription | Psoas Muscle | Psoas |
5 | chr9:15814800-15815400 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
6 | chr9:15814800-15831200 | Weak transcription | Psoas Muscle | Psoas |
7 | chr9:15815000-15815200 | ZNF genes & repeats | Primary hematopoietic stem cells | blood |
8 | chr9:15815000-15815200 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
9 | chr9:15815000-15815400 | Active TSS | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
10 | chr9:15816400-15818400 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
11 | chr9:15816800-15817200 | Weak transcription | Thymus | Thymus |
12 | chr9:15817000-15817400 | ZNF genes & repeats | Stomach Smooth Muscle | stomach |
13 | chr9:15817200-15817600 | ZNF genes & repeats | Thymus | Thymus |
14 | chr9:15824400-15825200 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
15 | chr9:15825200-15826600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
16 | chr9:15826400-15827000 | Enhancers | Brain Cingulate Gyrus | brain |
17 | chr9:15826400-15827000 | Enhancers | Brain Hippocampus Middle | brain |
18 | chr9:15826600-15827000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
19 | chr9:15827000-15834600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
20 | chr9:15828200-15828800 | Enhancers | Muscle Satellite Cultured Cells | -- |
21 | chr9:15830200-15857200 | Weak transcription | Primary hematopoietic stem cells | blood |