| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40044121-40044346 | Common:2; Rare:50 | ||||
| chr22:40044552-40044866 | Common:2; Rare:71 | ||||
| chr22:40346441-40346556 | Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40370438-40370670 | Rare:90 | ||||
| chr22:40636647-40637012 | Common:2; Rare:101 | ||||
| chr22:40856485-40857154 | Common:2; Rare:272; Clinvar:3 | ||||
| chr22:40951598-40951716 | Common:1; Rare:34 | ||||
| chr22:41091413-41091821 | Common:6; Rare:144 | ||||
| chr22:41286158-41286414 | Common:2; Rare:78 | ||||
| chr22:41301328-41301650 | Common:1; Rare:91 | ||||
| chr22:41367193-41367455 | Rare:80 | ||||
| chr22:41381818-41382026 | Common:3; Rare:87 | ||||
| chr22:41468649-41468810 | Common:2; Rare:46 | ||||
| chr22:41468997-41469149 | Rare:49 | ||||
| chr22:41544377-41544650 | Common:7; Rare:99 |