Variant report
| Variant | rs16938489 |
|---|---|
| Chromosome Location | chr8:49582495-49582496 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:49570000-49584000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr8:49573400-49586000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr8:49580200-49586600 | Enhancers | Fetal Lung | lung |
| 4 | chr8:49581200-49587800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 5 | chr8:49581600-49582800 | Weak transcription | Ovary | ovary |
| 6 | chr8:49581600-49584000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 7 | chr8:49581600-49584200 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
| 8 | chr8:49581600-49584400 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 9 | chr8:49581800-49582800 | Weak transcription | Fetal Stomach | stomach |
| 10 | chr8:49582000-49584600 | Enhancers | Fetal Kidney | kidney |
| 11 | chr8:49582200-49583200 | Enhancers | Aorta | Aorta |
| 12 | chr8:49582200-49584400 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 13 | chr8:49582400-49583600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
