Variant report
Variant | esv3419851 |
---|---|
Chromosome Location | chr1:195858329-195862327 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:9)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:9 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:195859567..195862131-chr1:195863598..195866284,2 | K562 | blood: | |
2 | chr1:195845835..195848707-chr1:195860208..195862083,2 | K562 | blood: | |
3 | chr1:195857673..195860102-chr1:195861318..195863869,3 | K562 | blood: | |
4 | chr1:195845835..195848328-chr1:195860583..195862092,2 | K562 | blood: | |
5 | chr1:195857673..195860102-chr1:195861318..195863869,3 | K562 | blood: | |
6 | chr1:195854670..195856185-chr1:195857598..195860308,2 | K562 | blood: | |
7 | chr1:195837170..195839918-chr1:195861015..195863064,2 | K562 | blood: | |
8 | chr1:195851101..195853777-chr1:195856895..195858997,3 | K562 | blood: | |
9 | chr1:195834331..195836964-chr1:195857452..195860455,3 | K562 | blood: |
No data |
No data |
No data |
No data |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs68003289 | chr1:195858335-195858336 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs6143550 | chr1:195858343-195858344 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs58141074 | chr1:195858344-195858345 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs57442041 | chr1:195858345-195858346 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs397719244 | chr1:195858354-195858355 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs368584293 | chr1:195858355-195858356 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs372889102 | chr1:195858356-195858357 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs530529690 | chr1:195858380-195858381 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs74963931 | chr1:195858390-195858391 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs570601298 | chr1:195858400-195858401 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs535215062 | chr1:195858428-195858429 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs752877 | chr1:195858446-195858447 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
13 | rs568693232 | chr1:195858452-195858453 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs535740214 | chr1:195858489-195858490 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs369859776 | chr1:195858505-195858506 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs187990002 | chr1:195858520-195858521 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs569111880 | chr1:195858605-195858606 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs539870129 | chr1:195858687-195858688 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs78296226 | chr1:195858699-195858700 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs35407587 | chr1:195858711-195858712 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs548665252 | chr1:195858744-195858745 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs573037879 | chr1:195858750-195858751 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs190770154 | chr1:195858753-195858754 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs540809414 | chr1:195858798-195858799 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Breast cancer | 17603634 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Schizophrenia | 19415332 | CNVD |
Autism | 22495311 | CNVD |
Liposarcoma | 21253554 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Melanoma | 18172304 | CNVD |
Rett syndrome | 21593744 | CNVD |
Cancer | 20164919 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Acute lymphoblastic leukemia | 17443227 | CNVD |
Wilms tumour | 21544195 | CNVD |
Breast cancer | 17133270 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Cervical cancer | 21063398 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 20632083 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Gastrointestinal stromal cancer | 20470368 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Medulloblastoma | 21292688 | CNVD |
Phyllodes tumor | 17334353 | CNVD |
Breast cancer | 21264507 | CNVD |
Multiple myeloma | 21628407 | CNVD |
Cancer | 16751803 | CNVD |
Prostate cancer | 16705090 | CNVD |
Neuroblastoma | 19435921 | CNVD |
Breast cancer | 17850661 | CNVD |
Breast cancer | 16461572 | CNVD |
Intracranial tumor | 16823260 | CNVD |
Medulloblastoma | 18056178 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Primary mediastinal b-cell lymphoma | 17728785 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Acute lymphoblastic leukemia | 21098271 | CNVD |
Neuroblastoma | 21899760 | CNVD |
Ovarian neoplasms | 16753589 | CNVD |
Glioblastoma multiforme | 17002787 | CNVD |
Breast cancer | 21858162 | CNVD |
Non-small cell lung cancer | 21385341 | CNVD |
Acute lymphoblastic leukemia | 21980252 | CNVD |
Breast cancer | 16608533 | CNVD |
Ewing''s sarcoma | 22429812 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Breast cancer | 17001317 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Prostate cancer | 18632612 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Testicular germ cell tumor | 18059402 | CNVD |
Ependymoma | 18628472 | CNVD |
Leukemia | 18628472 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Acute lymphoblastic leukemia | 19100363 | CNVD |
Breast cancer | 21509527 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Lung cancer | 18438408 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Melanoma | 20688739 | CNVD |
Breast cancer | 21611746 | CNVD |
primary effusion lymphomas | 17116491 | CNVD |
Breast cancer | 17393978 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Non-small cell lung cancer | 19010865 | CNVD |
Mental retardation | 17847001 | CNVD |
Basal cell lymphoma | 17170743 | CNVD |
Follicular lymphoma | 17170743 | CNVD |
Trisomy 5 syndrome | 21098271 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Breast cancer | 16272173 | CNVD |
Mental retardation | 21062444 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Chordoma | 18071362 | CNVD |
Breast cancer | 21364760 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Pancreatic ductal adenocarcinoma | 19077451 | CNVD |
Neuroblastoma | 20406844 | CNVD |
Breast cancer | 22522925 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:195858200-195858800 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |