| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40856431-40857159 | Common:2; Rare:297; Clinvar:3 | ||||
| chr22:40951031-40951423 | Common:2; Rare:134 | ||||
| chr22:40951600-40951716 | Common:1; Rare:34 | ||||
| chr22:41286122-41286448 | Common:2; Rare:105 | ||||
| chr22:41446790-41446963 | Rare:70 | ||||
| chr22:41468463-41468758 | Common:2; Rare:82 | ||||
| chr22:41469034-41469160 | Rare:50 | ||||
| chr22:41589794-41590146 | Common:6; Rare:127 | ||||
| chr22:41620992-41621385 | Common:7; Rare:141 | ||||
| chr22:41800542-41800688 | Common:1; Rare:42 | ||||
| chr22:41832908-41833209 | Common:3; Rare:99 | ||||
| chr22:41946736-41946949 | Common:3; Rare:52 | ||||
| chr22:41947089-41947203 | Rare:41 | ||||
| chr22:42079634-42079771 | Common:1; Rare:42 | ||||
| chr22:42090668-42090953 | Common:2; Rare:127; Clinvar (pathogenic):1 |