| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41468651-41468792 | Common:2; Rare:41 | ||||
| chr22:41468939-41469167 | Rare:74 | ||||
| chr22:41560924-41561139 | Common:9; Rare:65 | ||||
| chr22:41621057-41621390 | Common:6; Rare:118 | ||||
| chr22:41800536-41800688 | Common:1; Rare:46 | ||||
| chr22:41947093-41947203 | Rare:41 | ||||
| chr22:41998609-41998799 | Common:1; Rare:68 | ||||
| chr22:42070770-42071010 | Common:3; Rare:53 | ||||
| chr22:42079491-42079838 | Common:2; Rare:104 | ||||
| chr22:42090656-42091102 | Common:2; Rare:175; Clinvar (pathogenic):1 | ||||
| chr22:42210671-42210926 | Rare:77 | ||||
| chr22:42432364-42432511 | Rare:36 | ||||
| chr22:42614844-42615244 | Common:3; Rare:165 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:42857184-42857430 | Common:3; Rare:100 |