| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58278611-58278991 | Common:3; Rare:115 | ||||
| chr19:58326836-58327020 | Common:1; Rare:38 | ||||
| chr19:58327233-58327336 | Rare:25 | ||||
| chr19:58347614-58347774 | Common:7; Rare:77 | ||||
| chr19:58408430-58408678 | Common:3; Rare:79 | ||||
| chr19:58440134-58440434 | Common:5; Rare:80 | ||||
| chr19:58499206-58499552 | Common:2; Rare:115; Clinvar:5; Clinvar (benign):1 | ||||
| chr19:58519761-58520031 | Rare:71 | ||||
| chr19:58554939-58555210 | Common:2; Rare:86 | ||||
| chr19:58558893-58559150 | Common:1; Rare:81 | ||||
| chr19:58573535-58573629 | Common:1; Rare:27 | ||||
| chr2:264558-264964 | Common:4; Rare:146 | ||||
| chr2:677352-677557 | Common:1; Rare:87 | ||||
| chr2:3377791-3378035 | Common:2; Rare:68 | ||||
| chr2:3379608-3379761 | Common:1; Rare:62 |