Variant report
Variant | esv999705 |
---|---|
Chromosome Location | chr6:77439553-77455444 |
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 | rs71541138 | chr6:77439587-77439588 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
2 | rs13206329 | chr6:77439588-77439589 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
3 | rs577018334 | chr6:77439591-77439592 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
4 | rs370482157 | chr6:77439592-77439593 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
5 | rs2004871 | chr6:77439615-77439616 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
6 | rs562662980 | chr6:77439625-77439626 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
7 | rs561553920 | chr6:77439626-77439627 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
8 | rs529949675 | chr6:77439631-77439632 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
9 | rs548284283 | chr6:77439650-77439651 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
10 | rs2004870 | chr6:77439651-77439652 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
11 | rs527394337 | chr6:77439699-77439700 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
12 | rs551844696 | chr6:77439700-77439701 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
13 | rs1809246 | chr6:77439736-77439737 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
14 | rs538939758 | chr6:77439751-77439752 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
15 | rs114528932 | chr6:77439753-77439754 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
16 | rs114885806 | chr6:77439769-77439770 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
17 | rs536423595 | chr6:77439805-77439806 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
18 | rs181771316 | chr6:77439812-77439813 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
19 | rs112579852 | chr6:77439813-77439814 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
20 | rs184777053 | chr6:77439833-77439834 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
21 | rs4348275 | chr6:77439868-77439869 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
22 | rs188059629 | chr6:77439870-77439871 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
23 | rs112065728 | chr6:77439904-77439905 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
24 | rs181026598 | chr6:77439910-77439911 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
25 | rs562798915 | chr6:77439927-77439928 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
26 | rs574803101 | chr6:77439939-77439940 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
27 | rs137903486 | chr6:77439940-77439941 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
28 | rs571549518 | chr6:77439952-77439953 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
29 | rs752750 | chr6:77439969-77439970 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
30 | rs527347820 | chr6:77439990-77439991 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
31 | rs545926603 | chr6:77440047-77440048 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
32 | rs540312975 | chr6:77440063-77440064 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
33 | rs186339063 | chr6:77440106-77440107 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
34 | rs116646286 | chr6:77440107-77440108 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
35 | rs151120271 | chr6:77440153-77440154 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
36 | rs79747443 | chr6:77440154-77440155 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
37 | rs34659623 | chr6:77440155-77440156 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
38 | rs397886459 | chr6:77440172-77440173 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
39 | rs9443270 | chr6:77440190-77440191 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
40 | rs9443271 | chr6:77440204-77440205 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
41 | rs9447755 | chr6:77440215-77440216 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
42 | rs530337164 | chr6:77440249-77440250 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
43 | rs9443272 | chr6:77440256-77440257 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
44 | rs191244050 | chr6:77440266-77440267 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
45 | rs9443273 | chr6:77440296-77440297 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
46 | rs150161693 | chr6:77440310-77440311 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
47 | rs181313003 | chr6:77440318-77440319 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
48 | rs9443274 | chr6:77440335-77440336 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
49 | rs9443275 | chr6:77440341-77440342 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
50 | rs574742161 | chr6:77440365-77440366 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Uveal melanoma | 21693616 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Biliary cancer | 19435499 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Malaria | 21533027 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Autism | 21448237 | CNVD |
Breast cancer | 20668451 | CNVD |
Cancer | 20668451 | CNVD |
Lung cancer | 20668451 | CNVD |
Ovarian cancer | 20668451 | CNVD |
Pancreas cancer | 20668451 | CNVD |
Prostate cancer | 20668451 | CNVD |
Autism | 22495311 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Gastric cancer | 17908304 | CNVD |
Biliary cancer | 20360734 | CNVD |
Breast cancer | 20360734 | CNVD |
Coronary artery disease | 20360734 | CNVD |
Crohn''s disease | 20360734 | CNVD |
Hypertension | 20360734 | CNVD |
Rheumatoid arthritis | 20360734 | CNVD |
Type 1 diabetes | 20360734 | CNVD |
Type 2 diabetes | 20360734 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Breast cancer | 17603634 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Systemic lupus erythematosus | 17503323 | CNVD |
Melanoma | 18172304 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Cancer | 21637783 | CNVD |
Colorectal cancer | 16272173 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Acute lymphoblastic leukemia | 17443227 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Lung cancer | 18438408 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Follicular lymphoma | 19010834 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Breast cancer | 21264507 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Phyllodes tumor | 17334353 | CNVD |
Breast cancer | 16608533 | CNVD |
Non-small cell lung cancer | 21385341 | CNVD |
Prostate cancer | 16705090 | CNVD |
Adenoid cystic carcinoma | 17372589 | CNVD |
Ependymoma | 16718352 | CNVD |
High-proliferative meningiomas | 17937814 | CNVD |
Intracranial tumor | 16823260 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Prostate cancer | 16573809 | CNVD |
Breast cancer | 16272173 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Prostate cancer | 18632612 | CNVD |
Hodgkin''s lymphoma | 18641027 | CNVD |
Diffuse large b-cell lymphoma | 18287131 | CNVD |
Urothelial carcinoma | 18382360 | CNVD |
Ovarian neoplasms | 16753589 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Wilms tumour | 21544195 | CNVD |
Acute lymphoblastic leukemia | 21098271 | CNVD |
Follicular lymphoma | 17699855 | CNVD |
Breast cancer | 17133270 | CNVD |
Leukemia | 18688285 | CNVD |
Prostate cancer | 19242612 | CNVD |
Developmental delay | 21147756 | CNVD |
Glioma | 21046410 | CNVD |
Primary central nervous system lymphoma | 21088137 | CNVD |
Zellweger syndrome | 21572526 | CNVD |
Follicular lymphoma | 20505157 | CNVD |
Congenital diaphragmatic hernia | 21085971 | CNVD |
Malignant melanoma | 18718029 | CNVD |
low-grade B-cell lymphoma tumor | 18367492 | CNVD |
Lung adenocarcinoma | 21935476 | CNVD |
Breast cancer | 21364760 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Salivary gland tumor | 18059337 | CNVD |
Lung cancer | 16773561 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Urothelial cell carcinoma | 18451213 | CNVD |
Prostate cancer | 16461572 | CNVD |
Mental retardation | 21045960 | CNVD |
Obesity | 21045960 | CNVD |
learning difficulties | 21045960 | CNVD |
Prostate cancer | 17245344 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Invasive pancreatic ductal carcinoma | 16982739 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Cancer | 20164920 | CNVD |
Burkitt''s lymphoma | 20823134 | CNVD |
Ductal carcinoma | 22052326 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:77439200-77441000 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
2 | chr6:77441000-77452800 | Weak transcription | H1 Cell Line | embryonic stem cell |
3 | chr6:77443200-77443600 | Active TSS | Aorta | Aorta |
4 | chr6:77452400-77470200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
5 | chr6:77452800-77454400 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
6 | chr6:77454400-77456400 | Weak transcription | H1 Cell Line | embryonic stem cell |