Variant report
| Variant | rs73597600 |
|---|---|
| Chromosome Location | chr19:51501237-51501238 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr19:51496600-51502000 | Weak transcription | NHEK | skin |
| 2 | chr19:51496600-51503000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 3 | chr19:51498000-51502200 | Weak transcription | HMEC | breast |
| 4 | chr19:51498000-51503000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 5 | chr19:51499200-51501600 | Strong transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 6 | chr19:51499800-51503200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 7 | chr19:51500400-51502000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 8 | chr19:51501200-51501400 | Bivalent Enhancer | Primary mononuclear cells fromperipheralblood | Blood |
