Variant report
| Variant | rs73575832 |
|---|---|
| Chromosome Location | chr16:80073252-80073253 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr16:80062000-80075000 | Weak transcription | NH-A | brain |
| 2 | chr16:80064600-80073600 | Weak transcription | HMEC | breast |
| 3 | chr16:80070200-80074800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 4 | chr16:80070800-80074200 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 5 | chr16:80072200-80076000 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 6 | chr16:80072800-80073800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 7 | chr16:80072800-80085200 | Weak transcription | Esophagus | oesophagus |
| 8 | chr16:80073000-80074200 | Weak transcription | NHEK | skin |
| 9 | chr16:80073200-80078000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
