Variant report
Variant | esv3383447 |
---|---|
Chromosome Location | chr2:58896158-58896660 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:58890237..58893053-chr2:58893289..58896323,3 | K562 | blood: | |
2 | chr2:58894978..58898936-chr2:58901408..58904131,4 | K562 | blood: | |
3 | chr2:58893078..58896390-chr2:58901018..58903301,3 | K562 | blood: | |
4 | chr2:58896395..58898129-chr2:58901806..58903797,2 | 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 | rs541762516 | chr2:58896163-58896164 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
2 | rs560349590 | chr2:58896167-58896168 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
3 | rs76830679 | chr2:58896214-58896215 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
4 | rs72961965 | chr2:58896263-58896264 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
5 | rs564551897 | chr2:58896264-58896265 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
6 | rs560670082 | chr2:58896280-58896281 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
7 | rs564912547 | chr2:58896307-58896308 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
8 | rs376887438 | chr2:58896339-58896340 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
9 | rs531748672 | chr2:58896386-58896387 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
10 | rs371634236 | chr2:58896393-58896394 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
11 | rs149165434 | chr2:58896421-58896422 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
12 | rs547141204 | chr2:58896427-58896428 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
13 | rs112038866 | chr2:58896490-58896491 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
14 | rs368614770 | chr2:58896506-58896507 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
15 | rs567274252 | chr2:58896529-58896530 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
16 | rs547672674 | chr2:58896535-58896536 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
17 | rs6745423 | chr2:58896536-58896537 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
18 | rs144074801 | chr2:58896576-58896577 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
19 | rs185631916 | chr2:58896583-58896584 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
20 | rs72815812 | chr2:58896602-58896603 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
Disease | PMID | Source |
---|---|---|
Medulloblastoma | 21979893 | CNVD |
Lynch syndrome | 18415027 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Diffuse large b-cell lymphoma | 18287131 | CNVD |
Ovarian neoplasms | 16753589 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Neuroblastoma | 17533364 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Adrenal tumor | 17535989 | CNVD |
Breast cancer | 21264507 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Medulloblastoma | 17522785 | CNVD |
Cancer | 23418310 | CNVD |
Breast cancer | 17603634 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Ependymoma | 16718352 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Prostate cancer | 18632612 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Intellectual disability | 22102821 | CNVD |
Cancer | 20164919 | CNVD |
Hodgkin''s lymphoma | 18641027 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Follicular lymphoma | 20505157 | CNVD |
Autism | 17483303 | CNVD |
Myofibroblastic sarcoma | 19369631 | CNVD |
Esophageal adenocarcinoma | 18519675 | CNVD |
Medulloblastoma | 20607354 | CNVD |
Leukemia | 18628472 | CNVD |
Autism | 22495311 | CNVD |
Autism | 18522746 | CNVD |
Breast cancer | 21785460 | CNVD |
Lung cancer | 18438408 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Neuroblastoma | 21508638 | CNVD |
Neurodevelopmental disorder | 22521361 | CNVD |
Melanoma | 18172304 | CNVD |
Cancer | 16751803 | CNVD |
Colorectal cancer | 16272173 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Breast cancer | 16272173 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Ovarian cancer | 21720365 | CNVD |
abnormal development | 18461090 | CNVD |
Retinoblastoma | 22278416 | CNVD |
Cancer | 21183584 | CNVD |
Breast cancer | 16397240 | CNVD |
Chronic lymphocytic leukemia | 17053054 | CNVD |
Hereditary non-polyposis colorectal cancer | 19566914 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Acute lymphoblastic leukemia | 21980252 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Developmental delay | 21147756 | CNVD |
Mental retardation | 19951919 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Microcephaly | 20799320 | CNVD |
camptodactyly | 20799320 | CNVD |
cognitive delay | 20799320 | CNVD |
prenatal and postnatal growth deficiency | 20799320 | CNVD |
ptosis of eyelids | 20799320 | CNVD |
Maculopathy | 20981449 | CNVD |
2p16.1 microdeletion syndrome | 22283845 | CNVD |
Autism | 22579565 | CNVD |
Autism | 16963482 | CNVD |
Autism | 21750575 | CNVD |
idiopathic intellectual disability | 16963482 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Multiple myeloma | 16616336 | CNVD |
Follicular lymphoma | 17699855 | CNVD |
low-grade B-cell lymphoma tumor | 18367492 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Seminomas | 18059402 | CNVD |
Testicular germ cell tumor | 18059402 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:58896000-58897600 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |