| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38681847-38682026 | Common:1; Rare:80 | ||||
| chr22:40044525-40044862 | Common:2; Rare:80 | ||||
| chr22:40346434-40346556 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40856957-40857154 | Rare:86; Clinvar:3 | ||||
| chr22:41286164-41286447 | Common:2; Rare:86 | ||||
| chr22:41468638-41468772 | Common:2; Rare:37 | ||||
| chr22:41469054-41469149 | Rare:39 | ||||
| chr22:41620988-41621380 | Common:7; Rare:140 | ||||
| chr22:41832861-41833137 | Common:3; Rare:87 | ||||
| chr22:42070782-42070935 | Common:1; Rare:30 | ||||
| chr22:42079511-42079783 | Common:2; Rare:74 | ||||
| chr22:42090679-42090945 | Common:2; Rare:119; Clinvar (pathogenic):1 | ||||
| chr22:42614856-42615259 | Common:3; Rare:175 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:43015063-43015384 | Common:2; Rare:128 |