Variant report
Variant | esv1806861 |
---|---|
Chromosome Location | chr11:119952298-119956750 |
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 | rs573828041 | chr11:119952298-119952299 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs78642088 | chr11:119952299-119952300 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs2924345 | chr11:119952303-119952304 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs2924344 | chr11:119952304-119952305 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs532962086 | chr11:119952305-119952306 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs3017076 | chr11:119952310-119952311 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs78986249 | chr11:119952311-119952312 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs563363953 | chr11:119952313-119952314 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs111939733 | chr11:119952325-119952326 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs530665703 | chr11:119952328-119952329 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs549282076 | chr11:119952342-119952343 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs567863180 | chr11:119952357-119952358 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs199661497 | chr11:119952425-119952426 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs534965183 | chr11:119952426-119952427 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs546890757 | chr11:119952431-119952432 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs571652937 | chr11:119952453-119952454 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs538636002 | chr11:119952484-119952485 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs556968244 | chr11:119952485-119952486 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
19 | rs372323829 | chr11:119952500-119952501 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
20 | rs183040507 | chr11:119952513-119952514 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
21 | rs555239577 | chr11:119952569-119952570 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs573792560 | chr11:119952601-119952602 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
23 | rs541282579 | chr11:119952605-119952606 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
24 | rs375567761 | chr11:119952633-119952634 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
25 | rs200778706 | chr11:119952641-119952642 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs202138027 | chr11:119952688-119952689 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs578029410 | chr11:119952694-119952695 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs595061 | chr11:119952696-119952697 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs200454267 | chr11:119952697-119952698 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs545006927 | chr11:119952708-119952709 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs72455698 | chr11:119952719-119952720 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs373367472 | chr11:119952732-119952733 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs375972704 | chr11:119952743-119952744 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs372979724 | chr11:119952744-119952745 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs368977530 | chr11:119952769-119952770 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs79660778 | chr11:119952781-119952782 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs372968405 | chr11:119952806-119952807 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
38 | rs563301015 | chr11:119952841-119952842 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
39 | rs56104642 | chr11:119952842-119952843 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs530488261 | chr11:119952859-119952860 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs542715517 | chr11:119952885-119952886 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs561277789 | chr11:119952909-119952910 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
43 | rs1787019 | chr11:119952914-119952915 | ZNF genes & repeats Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
44 | rs546829021 | chr11:119952930-119952931 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs117991482 | chr11:119952937-119952938 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs571590561 | chr11:119952950-119952951 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
47 | rs146359191 | chr11:119952953-119952954 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
48 | rs550530511 | chr11:119952961-119952962 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
49 | rs188848603 | chr11:119952962-119952963 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
50 | rs536310664 | chr11:119952965-119952966 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Medulloblastoma | 21979893 | CNVD |
Gastric cancer | 17908304 | CNVD |
Multiple myeloma | 20724749 | CNVD |
Wilms tumour | 21544195 | CNVD |
Intellectual disability | 22102821 | CNVD |
Autism | 22495311 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Cancer | 21637783 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Chronic lymphocytic leukemia | 21795749 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Neuroblastoma | 21484798 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Oral cancer | 21386901 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Breast cancer | 20837533 | CNVD |
Breast cancer | 21264507 | CNVD |
Cervical cancer | 21063398 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Liposarcoma | 21253554 | CNVD |
Neuroblastoma | 18923524 | CNVD |
Neuroblastoma | 18664255 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Neuroblastoma | 17533364 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Cancer | 16751803 | CNVD |
Seminomas | 18059402 | CNVD |
Cervical cancer | 21062161 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Acute lymphoblastic leukemia | 21339820 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Cancer | 22429812 | CNVD |
Breast cancer | 16608533 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Melanoma | 18172304 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Basal cell lymphoma | 17053054 | CNVD |
Hepatocellular carcinoma | 16785998 | CNVD |
Breast cancer | 21858162 | CNVD |
Breast cancer | 21785460 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Breast cancer | 21958427 | CNVD |
Lung cancer | 18438408 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Breast cancer | 17133270 | CNVD |
Acute lymphoblastic leukemia | 21098271 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Breast cancer | 17603634 | CNVD |
Breast cancer | 21364760 | CNVD |
Mental retardation | 19966786 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
Invasive pancreatic ductal carcinoma | 16982739 | CNVD |
Ovarian cancer | 21720365 | CNVD |
Chronic lymphocytic leukemia | 18922857 | CNVD |
Neuroblastoma | 17327916 | CNVD |
Malignant melanoma | 17260012 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Prostate cancer | 16573809 | CNVD |
Prostate cancer | 18632612 | CNVD |
Renal cell carcinoma | 21668985 | CNVD |
Developmental delay | 21147756 | CNVD |
Emanuel syndrome | 21549014 | CNVD |
Emanuel syndrome | 18184694 | CNVD |
Non-syndromic sensorineural hearing loss | 18184694 | CNVD |
Acute lymphoblastic leukemia | 22581003 | CNVD |
Ovarian neoplasms | 16753589 | CNVD |
Chronic lymphocytic leukemia | 21049055 | CNVD |
Cancer | 21183584 | CNVD |
Retinoblastoma | 22278416 | CNVD |
Myxofibrosarcoma | 16751306 | CNVD |
Non-syndromic sensorineural hearing loss | 16829213 | CNVD |
Non-syndromic sensorineural hearing loss | 16760666 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
Renal cell carcinoma | 18765545 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Neurocytoma | 17123091 | CNVD |
Primary mediastinal b-cell lymphoma | 17728785 | CNVD |
Central neurocytomas | 17123091 | CNVD |
Congenital diaphragmatic hernia | 21525063 | CNVD |
Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
Multiple myeloma | 16616336 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Ovine squamous-cell carcinoma | 17599052 | CNVD |
Acute myeloid leukemia | 19651601 | CNVD |
Adenoid cystic carcinoma | 18698036 | CNVD |
Breast cancer | 20409316 | CNVD |
Salivary gland adenoid cystic carcinoma | 17545515 | CNVD |
Primary central nervous system lymphoma | 21088137 | CNVD |
Non-small cell lung cancer | 21385341 | CNVD |
Acute lymphoblastic leukemia | 17443227 | CNVD |
Heart disease | 20551144 | CNVD |
Malignant fibrous histiocytomas | 21085701 | CNVD |
Non-syndromic sensorineural hearing loss | 18496225 | CNVD |
Autism | 22543975 | CNVD |
Pancreatic ductal adenocarcinoma | 19077451 | CNVD |
Breast cancer | 21509527 | CNVD |
Ductal carcinoma | 22052326 | CNVD |
Schizophrenia | 23813976 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:119950400-119956400 | Weak transcription | Brain Substantia Nigra | brain |
2 | chr11:119950800-119954600 | Weak transcription | Brain Inferior Temporal Lobe | brain |
3 | chr11:119950800-119956400 | Weak transcription | Brain Hippocampus Middle | brain |
4 | chr11:119951200-119956400 | Weak transcription | Brain Cingulate Gyrus | brain |
5 | chr11:119951600-119953200 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
6 | chr11:119951800-119953400 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
7 | chr11:119953400-119954400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
8 | chr11:119954400-119955000 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
9 | chr11:119954600-119955000 | ZNF genes & repeats | iPS-18 Cell Line | embryonic stem cell |
10 | chr11:119954600-119955000 | Enhancers | Brain Inferior Temporal Lobe | brain |
11 | chr11:119954800-119955000 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
12 | chr11:119954800-119955200 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
13 | chr11:119954800-119955200 | Bivalent Enhancer | Adipose Nuclei | Adipose |
14 | chr11:119955000-119956400 | Weak transcription | Brain Inferior Temporal Lobe | brain |
15 | chr11:119955200-119956200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
16 | chr11:119955400-119961000 | Weak transcription | Esophagus | oesophagus |
17 | chr11:119956200-119957200 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
18 | chr11:119956400-119959200 | Enhancers | Brain Angular Gyrus | brain |
19 | chr11:119956400-119959400 | Enhancers | Brain Anterior Caudate | brain |
20 | chr11:119956400-119959400 | Enhancers | Brain Hippocampus Middle | brain |
21 | chr11:119956400-119959400 | Enhancers | Brain Inferior Temporal Lobe | brain |
22 | chr11:119956400-119959400 | Enhancers | Brain Substantia Nigra | brain |
23 | chr11:119956400-119959800 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
24 | chr11:119956400-119962800 | Enhancers | Brain Cingulate Gyrus | brain |
25 | chr11:119956600-119957600 | Enhancers | Fetal Brain Male | brain |