| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:29267943-29268339 | Common:2; Rare:115 | ||||
| chr22:30266848-30267142 | Rare:53 | ||||
| chr22:30356868-30356983 | Common:1; Rare:38 | ||||
| chr22:30606975-30607195 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:31081154-31081328 | Common:1; Rare:43 | ||||
| chr22:31107459-31107717 | Common:2; Rare:83 | ||||
| chr22:31292425-31292611 | Common:1; Rare:37 | ||||
| chr22:31399467-31399655 | Rare:53 | ||||
| chr22:31496286-31496556 | Common:2; Rare:78 | ||||
| chr22:31753749-31754087 | Common:1; Rare:120 | ||||
| chr22:32042940-32043152 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr22:35299706-35299919 | Common:2; Rare:55 | ||||
| chr22:36481567-36481729 | Common:2; Rare:45 | ||||
| chr22:36529074-36529344 | Common:2; Rare:85 | ||||
| chr22:37199362-37199554 | Common:3; Rare:50 |