| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21159311-21159662 | Common:1; Rare:118 | ||||
| chr16:21159766-21159837 | Common:1; Rare:7 | ||||
| chr16:21159857-21159892 | Rare:5 | ||||
| chr16:21302522-21302766 | Common:1; Rare:61 | ||||
| chr16:21302992-21303292 | Rare:62 | ||||
| chr16:21599061-21599096 | Rare:2 | ||||
| chr16:21599146-21599909 | Common:4; Rare:242 | ||||
| chr16:21600058-21600246 | Common:1; Rare:39 | ||||
| chr16:21600272-21600662 | Rare:86 | ||||
| chr16:21952326-21952673 | Rare:65 | ||||
| chr16:21952924-21953624 | Common:1; Rare:165; Clinvar (benign):3 | ||||
| chr16:22007581-22007750 | Common:2; Rare:50 | ||||
| chr16:22007928-22008266 | Rare:99 | ||||
| chr16:22008357-22008447 | Rare:37 | ||||
| chr16:22205934-22206532 | Common:1; Rare:140 |