Variant report
| Variant | rs12000698 |
|---|---|
| Chromosome Location | chr9:104044077-104044078 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:104038200-104054000 | Weak transcription | Fetal Brain Male | brain |
| 2 | chr9:104039200-104050000 | Weak transcription | HepG2 | liver |
| 3 | chr9:104041400-104053000 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 4 | chr9:104043400-104053400 | Weak transcription | Brain Cingulate Gyrus | brain |
