Variant report
| Variant | rs61917799 |
|---|---|
| Chromosome Location | chr12:67489491-67489492 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:67486200-67489800 | Weak transcription | NHEK | skin |
| 2 | chr12:67486200-67490200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 3 | chr12:67486200-67490200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 4 | chr12:67486400-67489800 | Weak transcription | HMEC | breast |
| 5 | chr12:67489000-67490400 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 6 | chr12:67489400-67490800 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
| 7 | chr12:67489400-67491800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
