| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58155078-58155220 | Common:2; Rare:35 | ||||
| chr19:58183311-58183449 | Rare:47 | ||||
| chr19:58278740-58279010 | Common:3; Rare:85 | ||||
| chr19:58326873-58327071 | Common:1; Rare:47 | ||||
| chr19:58327234-58327350 | Rare:26 | ||||
| chr19:58347534-58347774 | Common:7; Rare:109 | ||||
| chr19:58408433-58408686 | Common:4; Rare:77 | ||||
| chr19:58440120-58440448 | Common:6; Rare:84 | ||||
| chr19:58466890-58467085 | Common:1; Rare:60 | ||||
| chr19:58499200-58499532 | Common:3; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:58519754-58520003 | Rare:63 | ||||
| chr19:58554953-58555212 | Common:2; Rare:81 | ||||
| chr19:58558891-58559150 | Common:1; Rare:82 | ||||
| chr19:58573271-58573661 | Common:2; Rare:97 | ||||
| chr2:46500-46812 | Common:2; Rare:94 |