Variant report
| Variant | rs10979200 |
|---|---|
| Chromosome Location | chr9:110848437-110848438 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:110837400-110848800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 2 | chr9:110847000-110851200 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 3 | chr9:110847000-110851400 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
| 4 | chr9:110847200-110855800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 5 | chr9:110847600-110848800 | Enhancers | K562 | blood |
| 6 | chr9:110848200-110856200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 7 | chr9:110848400-110850400 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
| 8 | chr9:110848400-110851400 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
