Variant report
| Variant | rs12380068 |
|---|---|
| Chromosome Location | chr9:110688276-110688277 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:110685400-110691800 | Weak transcription | Fetal Stomach | stomach |
| 2 | chr9:110687000-110694800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 3 | chr9:110688000-110688600 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 4 | chr9:110688000-110688600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 5 | chr9:110688200-110689400 | Enhancers | Primary monocytes fromperipheralblood | blood |
