Variant report
Variant | esv2583928 |
---|---|
Chromosome Location | chr1:46365411-46366935 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:46349975..46352089-chr1:46365133..46367847,2 | 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 | rs542035324 | chr1:46365431-46365432 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs557130289 | chr1:46365441-46365442 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs372470316 | chr1:46365455-46365456 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs7548617 | chr1:46365489-46365490 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
5 | rs75793818 | chr1:46365498-46365499 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs11211220 | chr1:46365501-46365502 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
7 | rs539129101 | chr1:46365521-46365522 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs76875643 | chr1:46365522-46365523 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs564436553 | chr1:46365530-46365531 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs531773357 | chr1:46365531-46365532 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs12120067 | chr1:46365532-46365533 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
12 | rs188362208 | chr1:46365565-46365566 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs181266424 | chr1:46365566-46365567 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs370973624 | chr1:46365694-46365695 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
15 | rs547549498 | chr1:46365709-46365710 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
16 | rs565952752 | chr1:46365713-46365714 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
17 | rs551673027 | chr1:46365746-46365747 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
18 | rs376169526 | chr1:46365758-46365759 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
19 | rs369364436 | chr1:46365765-46365766 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
20 | rs537892814 | chr1:46365781-46365782 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
21 | rs555961995 | chr1:46365791-46365792 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
22 | rs574441885 | chr1:46365820-46365821 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
23 | rs541583215 | chr1:46365837-46365838 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
24 | rs527998382 | chr1:46365844-46365845 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
25 | rs372719013 | chr1:46365845-46365846 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
26 | rs59051138 | chr1:46365867-46365868 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
27 | rs368232800 | chr1:46365868-46365869 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
28 | rs57756307 | chr1:46365873-46365874 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
29 | rs146796161 | chr1:46365993-46365994 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
30 | rs572278808 | chr1:46366013-46366014 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
31 | rs140601200 | chr1:46366025-46366026 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
32 | rs71653984 | chr1:46366077-46366078 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
33 | rs564422065 | chr1:46366118-46366119 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
34 | rs199804809 | chr1:46366126-46366127 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
35 | rs200792572 | chr1:46366127-46366128 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
36 | rs201776620 | chr1:46366129-46366130 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
37 | rs113968402 | chr1:46366149-46366150 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
38 | rs564437929 | chr1:46366294-46366295 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
39 | rs374930436 | chr1:46366383-46366384 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
40 | rs369676874 | chr1:46366401-46366402 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
41 | rs199941586 | chr1:46366436-46366437 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
42 | rs111928971 | chr1:46366464-46366465 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
43 | rs145736063 | chr1:46366481-46366482 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
44 | rs186832831 | chr1:46366578-46366579 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
45 | rs79978857 | chr1:46366599-46366600 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
46 | rs76307349 | chr1:46366600-46366601 | Weak transcription ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
47 | rs189919314 | chr1:46366617-46366618 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
48 | rs569836486 | chr1:46366655-46366656 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
49 | rs529358198 | chr1:46366699-46366700 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
50 | rs547486844 | chr1:46366706-46366707 | Weak transcription ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Acute lymphoblastic leukemia | 20067559 | CNVD |
Melanoma | 18172304 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Breast cancer | 17603634 | CNVD |
Soft tissue tumor | 16732325 | CNVD |
Papillary thyroid carcinoma | 21436994 | CNVD |
Adenoid cystic carcinoma | 18698036 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Wilms tumour | 21544195 | CNVD |
Coronary Disease | 20032323 | CNVD |
Prostate cancer | 21965145 | CNVD |
Stargardt''s disease | 17277736 | CNVD |
Neuroblastoma | 17897457 | CNVD |
Uveal melanoma | 21693616 | CNVD |
Cancer | 21637783 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Neuroblastoma | 21484798 | CNVD |
Non-syndromic sensorineural hearing loss | 22290220 | CNVD |
Liposarcoma | 21253554 | CNVD |
Breast cancer | 21264507 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Astrocytoma | 17387387 | CNVD |
Cancer | 21499728 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Oligodendroglial tumors | 17285580 | CNVD |
Neuroblastoma | 17535989 | CNVD |
Pheochromocytoma | 17535989 | CNVD |
Prostate cancer | 16705090 | CNVD |
Astrocytoma | 17934521 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Neuroblastoma | 18664255 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Gastrointestinal stromal cancer | 19259404 | CNVD |
Gastrointestinal stromal cancer | 20470368 | CNVD |
Gastrointestinal stromal cancer | 17535989 | CNVD |
Neuroblastoma | 17533364 | CNVD |
Paraganglioma | 17535989 | CNVD |
Pulmonary chondroma | 17535989 | CNVD |
Myofibroblastic sarcoma | 19369631 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Schizophrenia | 19415332 | CNVD |
Non-syndromic sensorineural hearing loss | 21030649 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Chronic myeloid leukemia | 21384125 | CNVD |
Prostate cancer | 18632612 | CNVD |
Autism | 22495311 | CNVD |
Non-small cell lung cancer | 21385341 | CNVD |
Gastrointestinal stromal cancer | 16982739 | CNVD |
Chordoma | 21602918 | CNVD |
Acute lymphoblastic leukemia | 17443227 | CNVD |
Multiple myeloma | 16461302 | CNVD |
Melanoma | 17363583 | CNVD |
Cancer | 21129771 | CNVD |
Autosomal dominant nocturnal frontal lobe epilepsy | 18472482 | CNVD |
Hirschsprung''s Disease | 21712996 | CNVD |
Non-small cell lung cancer | 20864512 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Thrombocytopenia-absent radius syndrome | 21933853 | CNVD |
Psychiatric disorder | 22848183 | CNVD |
Diffuse large b-cell lymphoma | 18287131 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Breast cancer | 20409316 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Lung cancer | 18438408 | CNVD |
Splenic marginal zone lymphoma | 21957467 | CNVD |
Breast cancer | 17393978 | CNVD |
Cervical cancer | 21062161 | CNVD |
Cancer | 21183584 | CNVD |
Uveal melanoma | 20484589 | CNVD |
Ovarian cancer | 22174824 | CNVD |
Muscle-eye-brain disease | 21572526 | CNVD |
Breast cancer | 21785460 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Breast cancer | 20680643 | CNVD |
Colorectal cancer | 19287155 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Breast cancer | 21364760 | CNVD |
Ovarian cancer | 17875760 | CNVD |
Breast cancer | 20668451 | CNVD |
Cancer | 20668451 | CNVD |
Lung cancer | 20668451 | CNVD |
Ovarian cancer | 20668451 | CNVD |
Pancreas cancer | 20668451 | CNVD |
Prostate cancer | 20668451 | CNVD |
Breast cancer | 22522925 | CNVD |
Pancreatic cancer | 17952125 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:46342200-46391200 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |
2 | chr1:46347400-46378400 | Weak transcription | Brain Germinal Matrix | brain |
3 | chr1:46349600-46369000 | Weak transcription | Dnd41 | blood |
4 | chr1:46350800-46378800 | Weak transcription | K562 | blood |
5 | chr1:46356400-46366200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
6 | chr1:46357800-46376600 | Weak transcription | Psoas Muscle | Psoas |
7 | chr1:46358000-46374400 | Weak transcription | Fetal Intestine Small | intestine |
8 | chr1:46358400-46378200 | Weak transcription | Right Atrium | heart |
9 | chr1:46358600-46367200 | Weak transcription | Liver | Liver |
10 | chr1:46358600-46367400 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
11 | chr1:46358600-46374400 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
12 | chr1:46358600-46377600 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
13 | chr1:46358600-46377600 | Weak transcription | HSMM | muscle |
14 | chr1:46358800-46367000 | Weak transcription | HepG2 | liver |
15 | chr1:46359000-46365600 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
16 | chr1:46359200-46378800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
17 | chr1:46362800-46366000 | Weak transcription | Fetal Heart | heart |
18 | chr1:46363000-46393800 | Weak transcription | A549 | lung |
19 | chr1:46364600-46372600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
20 | chr1:46365600-46367400 | ZNF genes & repeats | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
21 | chr1:46366000-46366600 | Enhancers | Fetal Heart | heart |
22 | chr1:46366200-46369400 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
23 | chr1:46366400-46366800 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
24 | chr1:46366600-46376200 | Weak transcription | Fetal Heart | heart |
25 | chr1:46366800-46367800 | ZNF genes & repeats | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |