| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44356645-44356817 | Common:1; Rare:31 | ||||
| chr19:44500494-44500625 | Common:1; Rare:37 | ||||
| chr19:44643766-44643921 | Rare:54 | ||||
| chr19:44748010-44748173 | Rare:33 | ||||
| chr19:44777766-44778227 | Common:1; Rare:160 | ||||
| chr19:44778237-44778269 | Rare:9 | ||||
| chr19:44954344-44954599 | Common:2; Rare:65 | ||||
| chr19:44954924-44955003 | Common:2; Rare:20 | ||||
| chr19:45038951-45039107 | Rare:55 | ||||
| chr19:45078968-45079325 | Common:3; Rare:79 | ||||
| chr19:45091583-45091793 | Common:1; Rare:55 | ||||
| chr19:45406340-45406649 | Common:1; Rare:67 | ||||
| chr19:45423502-45423653 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr19:45423821-45423952 | Common:2; Rare:32 | ||||
| chr19:45469203-45469490 | Rare:93 |