| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40538601-40538938 | Common:1; Rare:57 | ||||
| chr22:40651718-40651869 | Common:3; Rare:36 | ||||
| chr22:41073625-41073656 | Rare:5 | ||||
| chr22:41137480-41137762 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:41149660-41149728 | Rare:22 | ||||
| chr22:41160468-41160719 | Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:41320354-41320698 | Common:1; Rare:74 | ||||
| chr22:41325572-41325828 | Rare:66 | ||||
| chr22:41355823-41356046 | Common:1; Rare:70 | ||||
| chr22:41518529-41518658 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr22:41618923-41619137 | Rare:45 | ||||
| chr22:41694662-41694970 | Rare:43 | ||||
| chr22:41870968-41871147 | Rare:62 | ||||
| chr22:42042739-42043011 | Common:1; Rare:42 | ||||
| chr22:42211424-42211638 | Rare:63 |