| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40636651-40637033 | Common:2; Rare:106 | ||||
| chr22:40856917-40857167 | Common:2; Rare:102; Clinvar:4 | ||||
| chr22:40951131-40951413 | Common:2; Rare:91 | ||||
| chr22:41091413-41091841 | Common:6; Rare:158 | ||||
| chr22:41286158-41286533 | Common:2; Rare:117 | ||||
| chr22:41446778-41446958 | Rare:71 | ||||
| chr22:41620982-41621368 | Common:7; Rare:140 | ||||
| chr22:41800529-41800631 | Rare:31 | ||||
| chr22:41832840-41833137 | Common:3; Rare:94 | ||||
| chr22:42070775-42070971 | Common:2; Rare:41 | ||||
| chr22:42079604-42079754 | Common:1; Rare:46 | ||||
| chr22:42090607-42090967 | Common:2; Rare:151; Clinvar (pathogenic):1 | ||||
| chr22:42432345-42432557 | Rare:46 | ||||
| chr22:42614858-42615259 | Common:3; Rare:174 | ||||
| chr22:42649308-42649482 | Common:1; Rare:68 |