Variant report
Variant | esv3431177 |
---|---|
Chromosome Location | chr8:122149916-122151770 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-MTBP-2 | chr8:122149259-122150049 | NONHSAT128459 |
No data |
No data |
No data |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs564628981 | chr8:122149921-122149922 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
2 | rs184852069 | chr8:122149964-122149965 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
3 | rs532904730 | chr8:122149965-122149966 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
4 | rs546741022 | chr8:122149972-122149973 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
5 | rs566559969 | chr8:122149983-122149984 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
6 | rs538056461 | chr8:122151016-122151017 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs551329924 | chr8:122151020-122151021 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs189910488 | chr8:122151022-122151023 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs534244391 | chr8:122151032-122151033 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs553964480 | chr8:122151071-122151072 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs567781392 | chr8:122151196-122151197 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs143770935 | chr8:122151200-122151201 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs117057502 | chr8:122151260-122151261 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs576774239 | chr8:122151293-122151294 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs576030044 | chr8:122151338-122151339 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs181183710 | chr8:122151407-122151408 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs577564588 | chr8:122151413-122151414 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs185612962 | chr8:122151428-122151429 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs143128266 | chr8:122151462-122151463 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs529015633 | chr8:122151467-122151468 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs28787740 | chr8:122151475-122151476 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs542387600 | chr8:122151518-122151519 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs562359693 | chr8:122151559-122151560 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs531452953 | chr8:122151583-122151584 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs10109711 | chr8:122151594-122151595 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
26 | rs117790143 | chr8:122151601-122151602 | Genic enhancers Enhancers | n/a | n/a | Overlapped CNVs | n/a |
27 | rs56016499 | chr8:122151629-122151630 | Genic enhancers Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
28 | rs148233555 | chr8:122151632-122151633 | Genic enhancers Enhancers | n/a | n/a | Overlapped CNVs | n/a |
29 | rs567625837 | chr8:122151664-122151665 | Genic enhancers Enhancers | n/a | n/a | Overlapped CNVs | n/a |
30 | rs536758773 | chr8:122151665-122151666 | Genic enhancers Enhancers | n/a | n/a | Overlapped CNVs | n/a |
31 | rs556752947 | chr8:122151682-122151683 | Genic enhancers Enhancers | n/a | n/a | Overlapped CNVs | n/a |
32 | rs190770641 | chr8:122151683-122151684 | Genic enhancers Enhancers | n/a | n/a | Overlapped CNVs | n/a |
33 | rs539286560 | chr8:122151725-122151726 | Genic enhancers Enhancers | n/a | n/a | Overlapped CNVs | n/a |
34 | rs558977837 | chr8:122151728-122151729 | Genic enhancers Enhancers | n/a | n/a | Overlapped CNVs | n/a |
35 | rs572733328 | chr8:122151745-122151746 | Genic enhancers Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Medulloblastoma | 21979893 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Autism | 19415332 | CNVD |
Malaria | 21533027 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Gastric cancer | 17908304 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Breast cancer | 21245420 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Seminomas | 18059402 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Pancreatic cancer | 21811587 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Testicular cancer | 18059402 | CNVD |
Breast cancer | 17133270 | CNVD |
Breast cancer | 21509527 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Breast cancer | 21858162 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Acute lymphoblastic leukemia | 21248843 | CNVD |
abnormal development | 18461090 | CNVD |
Oral cancer | 21386901 | CNVD |
Uveal melanoma | 21693616 | CNVD |
Langer-Giedion syndrome | 22283845 | CNVD |
Cancer | 21637783 | CNVD |
Splenic marginal zone lymphoma | 21957467 | CNVD |
Breast cancer | 20632083 | CNVD |
Breast cancer | 17603634 | CNVD |
Breast cancer | 19602461 | CNVD |
Cancer | 22429812 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Oral cancer | 19627613 | CNVD |
Prostate cancer | 21088497 | CNVD |
colon cancer | 17210682 | CNVD |
Breast cancer | 21264507 | CNVD |
Breast cancer | 22028636 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Cancer | 16751803 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Gastric cancer | 17167181 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Breast cancer | 16461572 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Medulloblastoma | 16968546 | CNVD |
head and neck squamous cell carcinoma | 18028549 | CNVD |
Breast cancer | 17001317 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Lung cancer | 18438408 | CNVD |
Breast cancer | 16608533 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Prostate cancer | 18632612 | CNVD |
Ovarian cancer | 22174824 | CNVD |
Prostate cancer | 16573809 | CNVD |
Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Adenocarcinoma | 21044232 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
T-cell prolymphocytic leukemia | 17713554 | CNVD |
Prostate cancer | 16461572 | CNVD |
Breast cancer | 21399628 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Breast cancer | 17393978 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Non-syndromic sensorineural hearing loss | 20606397 | CNVD |
Breast cancer | 17899364 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Congenital diaphragmatic hernia | 21085971 | CNVD |
Breast cancer | 21611746 | CNVD |
Developmental delay | 21147756 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Congenital diaphragmatic hernia | 21525063 | CNVD |
Non-small cell lung cancer | 19010865 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Papillary thyroid cancer | 17515504 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Breast cancer | 20932292 | CNVD |
Gastric cancer | 22539939 | CNVD |
Breast cancer | 22056952 | CNVD |
Langer-Giedion syndrome | 16773131 | CNVD |
Lung cancer | 16740712 | CNVD |
Mental retardation | 16773131 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Langer-Giedion syndrome | 22470819 | CNVD |
Cornelia de Lange syndrome | 24599119 | CNVD |
Gastric cancer | 21528007 | CNVD |
Breast cancer | 22532251 | CNVD |
Cervical cancer | 21062161 | CNVD |
Cancer | 21129771 | CNVD |
benign familial neonatal convulsions | 18472482 | CNVD |
Breast cancer | 16417655 | CNVD |
Astrocytoma | 17387387 | CNVD |
Cancer | 21183584 | CNVD |
Follicular lymphoma | 20505157 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Medulloblastoma | 20607354 | CNVD |
Breast cancer | 20814816 | CNVD |
Colorectal cancer | 22486879 | CNVD |
Breast cancer | 17908964 | CNVD |
Colorectal cancer | 20031965 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Ovarian cancer | 17908964 | CNVD |
Ovarian cancer | 20031965 | CNVD |
Prostate cancer | 20031965 | CNVD |
Non-small cell lung cancer | 17643093 | CNVD |
Prostate cancer | 19242612 | CNVD |
Colorectal cancer | 16774939 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Glioblastoma multiforme | 18628472 | CNVD |
Malignant melanoma | 17260012 | CNVD |
Breast cancer | 18698023 | CNVD |
Multiple myeloma | 16461302 | CNVD |
Uveal melanoma | 20484589 | CNVD |
head and neck squamous cell carcinoma | 16740747 | CNVD |
Breast cancer | 19181860 | CNVD |
Endometrial cancer | 23636398 | CNVD |
Intracranial aneurysm | 16715129 | CNVD |
Breast cancer | 16397240 | CNVD |
Multiple myeloma | 16616336 | CNVD |
Diffuse large b-cell lymphoma | 18287131 | CNVD |
Breast cancer | 21364760 | CNVD |
Oral squamous cell carcinoma | 21853135 | CNVD |
Burkitt''s lymphoma | 20823134 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:122151000-122151600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr8:122151000-122151800 | Enhancers | HMEC | breast |
3 | chr8:122151600-122152200 | Genic enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |