| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58466879-58467110 | Common:1; Rare:73 | ||||
| chr19:58476023-58476433 | Common:1; Rare:134 | ||||
| chr19:58499166-58499648 | Common:3; Rare:170; Clinvar:7; Clinvar (benign):2 | ||||
| chr19:58519525-58519729 | Rare:46 | ||||
| chr19:58519754-58520031 | Rare:72 | ||||
| chr19:58550001-58550167 | Common:1; Rare:78 | ||||
| chr19:58558290-58558720 | Rare:137 | ||||
| chr19:58558916-58559145 | Common:1; Rare:70 | ||||
| chr19:58564128-58564170 | Rare:11 | ||||
| chr19:58564496-58564888 | Common:1; Rare:71 | ||||
| chr19:58573261-58573831 | Common:5; Rare:137 | ||||
| chr2:264530-265011 | Common:4; Rare:189 | ||||
| chr2:676623-677104 | Common:3; Rare:121 | ||||
| chr2:677334-677483 | Common:1; Rare:66 | ||||
| chr2:1744265-1744308 | Rare:13 |