| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58002796-58002922 | Common:1; Rare:61 | ||||
| chr19:58059164-58059287 | Rare:65 | ||||
| chr19:58098208-58098427 | Common:8; Rare:83 | ||||
| chr19:58278664-58278991 | Common:3; Rare:100 | ||||
| chr19:58326873-58327036 | Common:1; Rare:36 | ||||
| chr19:58327227-58327309 | Rare:20 | ||||
| chr19:58347520-58347777 | Common:8; Rare:113 | ||||
| chr19:58408466-58408686 | Common:3; Rare:66 | ||||
| chr19:58440134-58440457 | Common:6; Rare:88 | ||||
| chr19:58499211-58499545 | Common:2; Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:58519765-58520037 | Rare:71 | ||||
| chr19:58554931-58555210 | Common:2; Rare:90 | ||||
| chr2:677352-677557 | Common:1; Rare:87 | ||||
| chr2:3377766-3377996 | Rare:67 | ||||
| chr2:3379608-3379785 | Common:2; Rare:74 |