Variant report
Variant | nsv976267 |
---|---|
Chromosome Location | chr13:63320790-63340383 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:2)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:2 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-PCDH20-4 | chr13:63321740-63322054 | XLOC_010638 |
2 | lnc-PCDH20-4 | chr13:63321841-63322054 | NONHSAT034155 |
No data |
No data |
No data |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs546217355 | chr13:63321218-63321219 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs564801891 | chr13:63321240-63321241 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs576591161 | chr13:63321253-63321254 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs187127694 | chr13:63321311-63321312 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs190744248 | chr13:63321343-63321344 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs558883768 | chr13:63321346-63321347 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs182930889 | chr13:63321379-63321380 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs544749137 | chr13:63321407-63321408 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs116490434 | chr13:63321430-63321431 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs386771599 | chr13:63321440-63321441 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs532932217 | chr13:63321447-63321448 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs572305380 | chr13:63321454-63321455 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs551414887 | chr13:63321475-63321476 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs569917601 | chr13:63321496-63321497 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs537258549 | chr13:63321507-63321508 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs187954303 | chr13:63321584-63321585 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs141482617 | chr13:63321831-63321832 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
18 | rs80120702 | chr13:63321842-63321843 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
19 | rs560440058 | chr13:63321858-63321859 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
20 | rs2275125 | chr13:63321872-63321873 | Inactive region | lncRNA | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
21 | rs555493977 | chr13:63321932-63321933 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
22 | rs184478467 | chr13:63321934-63321935 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
23 | rs187764240 | chr13:63321978-63321979 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
24 | rs563341415 | chr13:63322022-63322023 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
25 | rs559377267 | chr13:63322041-63322042 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Prostate cancer | 16705090 | CNVD |
High-proliferative meningiomas | 17937814 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Intellectual disability | 22102821 | CNVD |
Cancer | 20164919 | CNVD |
Autism | 22495311 | CNVD |
Chordoma | 21602918 | CNVD |
Bladder cancer | 21949216 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Cancer | 21637783 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Chronic lymphocytic leukemia | 21518781 | CNVD |
colon cancer | 17210682 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 21264507 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Ovarian cancer | 20844748 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Intracranial aneurysm | 19064780 | CNVD |
Breast cancer | 19287154 | CNVD |
Acute myeloid leukemia | 18379011 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Olfactory neuroblastoma | 18408657 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Ependymoma | 16718352 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Colorectal cancer | 16272173 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Gastrointestinal stromal cancer | 16982739 | CNVD |
Breast cancer | 16608533 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Ovarian cancer | 22174824 | CNVD |
Breast cancer | 17133270 | CNVD |
Myoepithelioma | 18604193 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Acute lymphoblastic leukemia | 21098271 | CNVD |
Prostate cancer | 16573809 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Paraganglioma | 21461997 | CNVD |
Pheochromocytoma | 21461997 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Prostate cancer | 17245344 | CNVD |
Prostate cancer | 18632612 | CNVD |
Colorectal cancer | 21586687 | CNVD |
Small bowel adenocarcinoma | 21586687 | CNVD |
Retinoblastoma | 19183342 | CNVD |
Developmental delay | 21147756 | CNVD |
Melanoma | 18172304 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Merkel cell carcinoma | 19020549 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Non-syndromic sensorineural hearing loss | 18496225 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Breast cancer | 21858162 | CNVD |
Glioblastoma multiforme | 21922591 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Gastric cancer | 17908304 | CNVD |
Glioblastoma multiforme | 21750150 | CNVD |
Breast cancer | 17603634 | CNVD |
Cancer | 21183584 | CNVD |
Breast cancer | 17393978 | CNVD |
Splenic marginal zone lymphoma | 18492102 | CNVD |
Liposarcoma | 21253554 | CNVD |
Gastrointestinal stromal cancer | 20818650 | CNVD |
head and neck squamous cell carcinoma | 17671120 | CNVD |
Colorectal cancer | 16774939 | CNVD |
Adenoid cystic carcinoma | 17372589 | CNVD |
abnormal development | 18461090 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Chronic lymphocytic leukemia | 20421269 | CNVD |
Acute lymphoblastic leukemia | 21980252 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Anaplastic thyroid cancer | 18753363 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lung cancer | 18438408 | CNVD |
Bipolar disorder | 19114987 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:63321200-63321600 | Enhancers | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |