Variant report
Variant | esv2592040 |
---|---|
Chromosome Location | chr4:81990872-81992474 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:5 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr4:81990998..81991602-chr4:82272501..82273357,5 | MCF-7 | breast: | |
2 | chr4:81990984..81991561-chr4:83122784..83123414,2 | K562 | blood: | |
3 | chr4:81990594..81991584-chr4:82181118..82182501,8 | MCF-7 | breast: | |
4 | chr4:81990848..81991586-chr4:82272501..82273236,3 | K562 | blood: | |
5 | chr4:81990624..81991565-chr4:82272517..82273470,4 | 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 | rs564324503 | chr4:81990876-81990877 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs140401847 | chr4:81990878-81990879 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs532987831 | chr4:81990879-81990880 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs549548793 | chr4:81990893-81990894 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs7692471 | chr4:81990901-81990902 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
6 | rs75510140 | chr4:81990938-81990939 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs548567756 | chr4:81990953-81990954 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs149256429 | chr4:81990954-81990955 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs369762498 | chr4:81990980-81990981 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs554142645 | chr4:81990990-81990991 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs2685465 | chr4:81991016-81991017 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
12 | rs1495639 | chr4:81991027-81991028 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
13 | rs184924986 | chr4:81991036-81991037 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs576253601 | chr4:81991044-81991045 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs541905088 | chr4:81991050-81991051 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs79298551 | chr4:81991064-81991065 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs188646309 | chr4:81991097-81991098 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs192338291 | chr4:81991114-81991115 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs564257438 | chr4:81991120-81991121 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs533539879 | chr4:81991147-81991148 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs1845719 | chr4:81991150-81991151 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs1987331 | chr4:81991163-81991164 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs184452317 | chr4:81991173-81991174 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs563095204 | chr4:81991187-81991188 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs189611621 | chr4:81991232-81991233 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
26 | rs548359366 | chr4:81991297-81991298 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
27 | rs543389194 | chr4:81991371-81991372 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
28 | rs568463938 | chr4:81991372-81991373 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Acute lymphoblastic leukemia | 22237106 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Chordoma | 21602918 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Intellectual disability | 22102821 | CNVD |
Autism | 22495311 | CNVD |
Breast cancer | 21858162 | CNVD |
Small bowel adenocarcinoma | 21586687 | CNVD |
Gastric cancer | 21586687 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Melanoma | 18172304 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Breast cancer | 17603634 | CNVD |
Glioblastoma multiforme | 21922591 | CNVD |
Parkinson disease | 21956041 | CNVD |
Mental retardation | 20522426 | CNVD |
delayed speech | 20522426 | CNVD |
growth disorder | 20522426 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Myxofibrosarcoma | 16751306 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Parkinson disease | 18923514 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Cancer | 21183584 | CNVD |
Breast cancer | 16272173 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Malignant mesothelioma | 18160781 | CNVD |
Medulloblastoma | 18056178 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Pleural malignant mesothelioma | 18160781 | CNVD |
Primary mediastinal b-cell lymphoma | 17728785 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
4q-syndrome | 17576883 | CNVD |
Cancer | 21637783 | CNVD |
Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Muscular dystrophy | 21149563 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Breast cancer | 21264507 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 17387387 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Liposarcoma | 21253554 | CNVD |
Oligodendroglial tumors | 17285580 | CNVD |
Cervical cancer | 21062161 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Breast cancer | 16608533 | CNVD |
Adenoid cystic carcinoma | 18698036 | CNVD |
Lung cancer | 19208797 | CNVD |
Wilms tumour | 21544195 | CNVD |
Breast cancer | 21785460 | CNVD |
Basal cell lymphoma | 17170743 | CNVD |
Follicular lymphoma | 17170743 | CNVD |
Chronic lymphocytic leukemia | 20421269 | CNVD |
Myelodysplastic syndrome | 21251322 | CNVD |
Multiple myeloma | 17550852 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lung cancer | 18438408 | CNVD |
Chronic lymphocytic leukemia | 18922857 | CNVD |
Cancer | 22429812 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Autism | 18414403 | CNVD |
Chronic lymphocytic leukemia | 21670202 | CNVD |
primary effusion lymphomas | 17116491 | CNVD |
Gastric cancer | 16891809 | CNVD |
Prostate cancer | 16573809 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Neuroblastoma | 21899760 | CNVD |
Myelodysplastic syndrome | 18508791 | CNVD |
abnormal development | 18461090 | CNVD |
Breast cancer | 22522925 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:81990600-81991400 | Enhancers | NHDF-Ad | bronchial |
2 | chr4:81990800-81991000 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
3 | chr4:81990800-81991200 | Enhancers | Ovary | ovary |
4 | chr4:81990800-81991200 | Enhancers | NHLF | lung |
5 | chr4:81990800-81991400 | Enhancers | Foreskin Fibroblast Primary Cells skin01 | Skin |
6 | chr4:81990800-81991400 | Enhancers | Brain Cingulate Gyrus | brain |
7 | chr4:81990800-81991400 | Enhancers | Colon Smooth Muscle | Colon |
8 | chr4:81990800-81991400 | Enhancers | Fetal Brain Female | brain |
9 | chr4:81990800-81991400 | Enhancers | Rectal Smooth Muscle | rectum |
10 | chr4:81990800-81991400 | Enhancers | Stomach Smooth Muscle | stomach |