Variant report
Variant | esv3327534 |
---|---|
Chromosome Location | chr3:28856048-28859846 |
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)
No data |
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No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs544348396 | chr3:28856078-28856079 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs1604070 | chr3:28856091-28856092 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
3 | rs187835610 | chr3:28856163-28856164 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs544875360 | chr3:28856171-28856172 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs9830243 | chr3:28856181-28856182 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
6 | rs578260266 | chr3:28856218-28856219 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs74980672 | chr3:28856219-28856220 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs560552543 | chr3:28856232-28856233 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs528967951 | chr3:28856243-28856244 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs548826567 | chr3:28856283-28856284 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs540827069 | chr3:28856284-28856285 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs560452683 | chr3:28856302-28856303 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs192427738 | chr3:28856344-28856345 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs183204791 | chr3:28856403-28856404 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs551002450 | chr3:28856420-28856421 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs571202413 | chr3:28856465-28856466 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs533860911 | chr3:28856473-28856474 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs547171712 | chr3:28856563-28856564 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs78426273 | chr3:28856588-28856589 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Chronic lymphocytic leukemia | 21546498 | CNVD |
Breast cancer | 17603634 | CNVD |
Neuroblastoma | 17327916 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Colorectal cancer | 21297112 | CNVD |
Lynch syndrome | 18415027 | CNVD |
Renal cell carcinoma | 18592004 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Urothelial carcinoma | 18382360 | CNVD |
Melanoma | 18172304 | CNVD |
Cervical cancer | 21062161 | CNVD |
Hirschsprung''s Disease | 21712996 | CNVD |
head and neck squamous cell carcinoma | 17671120 | CNVD |
Insulin resistance | 16721378 | CNVD |
Neuroblastoma | 18664255 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Neuroblastoma | 21484798 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
Oral cancer | 19627613 | CNVD |
Renal cell carcinoma | 19461508 | CNVD |
Epithelial cancer | 22065749 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Liposarcoma | 21253554 | CNVD |
Basal cell lymphoma | 21115979 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Pancreatic endocrine tumor | 20981439 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 21264507 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Oral cancer | 21386901 | CNVD |
Cutaneous squamous cell carcinomas | 19131950 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Uveal melanoma | 21693616 | CNVD |
Retinoblastoma | 21504564 | CNVD |
T-cell prolymphocytic leukemia | 17713554 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Renal cell carcinoma | 21668985 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Lung cancer | 20668451 | CNVD |
Breast cancer | 20668451 | CNVD |
Cancer | 20668451 | CNVD |
Ovarian cancer | 20668451 | CNVD |
Pancreas cancer | 20668451 | CNVD |
Prostate cancer | 20668451 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lung cancer | 18438408 | CNVD |
Intellectual disability | 22102821 | CNVD |
Esophageal cancer | 20955586 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Myofibroblastic sarcoma | 19369631 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
Breast cancer | 17133270 | CNVD |
Uveal melanoma | 20484589 | CNVD |
Autism | 22495311 | CNVD |
Melanoma | 20688739 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Lung cancer | 16618734 | CNVD |
Cancer | 20164919 | CNVD |
Developmental delay | 21147756 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:28856000-28856600 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |