| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38831721-38832061 | Common:4; Rare:113; Clinvar (benign):1 | ||||
| chr19:38899517-38900063 | Rare:165 | ||||
| chr19:38930737-38931023 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39335973-39336186 | Rare:58 | ||||
| chr19:39390947-39391432 | Common:1; Rare:181 | ||||
| chr19:39406699-39406955 | Rare:105 | ||||
| chr19:39407503-39407831 | Common:1; Rare:82 | ||||
| chr19:39445485-39445759 | Common:2; Rare:74 | ||||
| chr19:39846317-39846487 | Common:1; Rare:80 | ||||
| chr19:39970918-39971238 | Common:4; Rare:90 | ||||
| chr19:39996944-39997093 | Common:5; Rare:51 | ||||
| chr19:40056147-40056330 | Rare:27 | ||||
| chr19:40090871-40090974 | Common:1; Rare:31 | ||||
| chr19:40280801-40280937 | Rare:28 | ||||
| chr19:40285183-40285492 | Common:1; Rare:106 |