Variant report
Variant | nsv1043757 |
---|---|
Chromosome Location | chr10:83247947-83351242 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:6)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:6 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr10:83272245..83276354-chr10:83281692..83284767,3 | MCF-7 | breast: | |
2 | chr10:83257478..83259594-chr10:83260723..83262916,2 | MCF-7 | breast: | |
3 | chr10:83273413..83276377-chr10:83278603..83280338,2 | K562 | blood: | |
4 | chr10:83273413..83276377-chr10:83278603..83280338,2 | K562 | blood: | |
5 | chr10:83272245..83276354-chr10:83281692..83284767,3 | MCF-7 | breast: | |
6 | chr10:83257478..83259594-chr10:83260723..83262916,2 | MCF-7 | breast: |
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 | rs577456360 | chr10:83258019-83258020 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs112846754 | chr10:83258040-83258041 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs35456328 | chr10:83258046-83258047 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs556347295 | chr10:83258056-83258057 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs2346519 | chr10:83258059-83258060 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
6 | rs541723874 | chr10:83258077-83258078 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs541147992 | chr10:83258117-83258118 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs562036041 | chr10:83258204-83258205 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs77216998 | chr10:83258232-83258233 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs76851415 | chr10:83258233-83258234 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs527268761 | chr10:83258249-83258250 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs539587974 | chr10:83258288-83258289 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs12269509 | chr10:83258298-83258299 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs540657820 | chr10:83258350-83258351 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs75232893 | chr10:83258355-83258356 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs532907328 | chr10:83258358-83258359 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs113429844 | chr10:83258367-83258368 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs530481356 | chr10:83258408-83258409 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs7072690 | chr10:83258436-83258437 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs531956213 | chr10:83258498-83258499 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs577582190 | chr10:83258523-83258524 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs548581414 | chr10:83258532-83258533 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs568771073 | chr10:83258544-83258545 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs533933076 | chr10:83258599-83258600 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs575601637 | chr10:83262618-83262619 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
26 | rs532728442 | chr10:83262624-83262625 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
27 | rs2103856 | chr10:83262625-83262626 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
28 | rs574660910 | chr10:83262630-83262631 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
29 | rs540476373 | chr10:83262632-83262633 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
30 | rs560465306 | chr10:83262648-83262649 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
31 | rs532403875 | chr10:83262656-83262657 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
32 | rs546131175 | chr10:83262657-83262658 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
33 | rs377287763 | chr10:83262658-83262659 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
34 | rs375340968 | chr10:83262679-83262680 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
35 | rs116447521 | chr10:83262697-83262698 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
36 | rs547956593 | chr10:83262707-83262708 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
37 | rs185993018 | chr10:83262708-83262709 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
38 | rs73305463 | chr10:83262715-83262716 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
39 | rs569374637 | chr10:83262734-83262735 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
40 | rs374656483 | chr10:83262760-83262761 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
41 | rs574678104 | chr10:83262771-83262772 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
42 | rs555656883 | chr10:83262777-83262778 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
43 | rs140211317 | chr10:83262779-83262780 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
44 | rs569126302 | chr10:83262780-83262781 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
45 | rs538264408 | chr10:83262788-83262789 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
46 | rs117426760 | chr10:83262790-83262791 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
47 | rs79434870 | chr10:83262791-83262792 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
48 | rs189321911 | chr10:83262814-83262815 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
49 | rs553971070 | chr10:83262841-83262842 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
50 | rs577127568 | chr10:83262843-83262844 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Gastric cancer | 17908304 | CNVD |
Chordoma | 21602918 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Melanoma | 18172304 | CNVD |
Pleomorphic xanthoastrocytoma | 20730472 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Acute lymphoblastic leukemia | 20724749 | CNVD |
Autism | 22495311 | CNVD |
Prostate cancer | 18632612 | CNVD |
Cockayne syndrome | 18421352 | CNVD |
Glioblastoma | 16823260 | CNVD |
Medulloblastoma | 16968546 | CNVD |
Neuroblastoma | 17533364 | CNVD |
Squamous cell cancer | 21044232 | CNVD |
Glioma | 21971842 | CNVD |
Cancer | 21637783 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Breast cancer | 21264507 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Liposarcoma | 21253554 | CNVD |
Oligodendroglial tumors | 17285580 | CNVD |
Lung cancer | 18438408 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Usher syndrome | 20538994 | CNVD |
Medulloblastoma | 16783165 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Breast cancer | 21785460 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Prostate cancer | 16573809 | CNVD |
Paraganglioma | 17535989 | CNVD |
Submicroscopic aberration syndrome | 21292638 | CNVD |
Gastrointestinal stromal cancer | 17535989 | CNVD |
Pancreatic endocrine tumor | 17639061 | CNVD |
Pulmonary chondroma | 17535989 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Colorectal cancer | 18645599 | CNVD |
Polyposis syndrome | 18645599 | CNVD |
Prostate cancer | 17245344 | CNVD |
Glioblastoma multiforme | 17369134 | CNVD |
Glioblastoma multiforme | 21750150 | CNVD |
Breast cancer | 22032731 | CNVD |
Ovarian cancer | 20844748 | CNVD |
Glioblastoma multiforme | 17002787 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 17603634 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Breast cancer | 21364760 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
early-passage human iPS cells | 21368824 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:83258000-83258600 | Enhancers | Fetal Kidney | kidney |
2 | chr10:83262600-83263000 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr10:83274200-83275000 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr10:83274200-83275200 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
5 | chr10:83274800-83275200 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
6 | chr10:83290000-83290200 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
7 | chr10:83291600-83293800 | Enhancers | Liver | Liver |
8 | chr10:83307800-83308400 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
9 | chr10:83308200-83308800 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
10 | chr10:83323800-83324400 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
11 | chr10:83328200-83330200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
12 | chr10:83328400-83329800 | Enhancers | Brain Germinal Matrix | brain |
13 | chr10:83330200-83331200 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
14 | chr10:83331000-83331200 | Enhancers | H1 Derived Mesenchymal Stem Cells | ES cell derived |