| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58183311-58183441 | Rare:45 | ||||
| chr19:58228857-58228955 | Rare:32 | ||||
| chr19:58278611-58278998 | Common:4; Rare:118 | ||||
| chr19:58326875-58327048 | Common:1; Rare:42 | ||||
| chr19:58327226-58327317 | Rare:22 | ||||
| chr19:58347520-58347762 | Common:7; Rare:107 | ||||
| chr19:58401233-58401538 | Common:5; Rare:92 | ||||
| chr19:58440139-58440338 | Common:5; Rare:50 | ||||
| chr19:58466915-58467085 | Rare:56 | ||||
| chr19:58499211-58499545 | Common:2; Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:58519771-58520011 | Rare:65 | ||||
| chr19:58554195-58554310 | Rare:38 | ||||
| chr19:58554950-58555183 | Common:1; Rare:77 | ||||
| chr19:58573461-58573598 | Common:1; Rare:35 | ||||
| chr2:677352-677557 | Common:1; Rare:87 |