| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40636629-40637033 | Common:2; Rare:116 | ||||
| chr22:40819283-40819514 | Common:11; Rare:109 | ||||
| chr22:40856364-40857169 | Common:4; Rare:331; Clinvar:4 | ||||
| chr22:40951022-40951413 | Common:2; Rare:136 | ||||
| chr22:40951574-40951716 | Common:2; Rare:46 | ||||
| chr22:41091413-41091825 | Common:6; Rare:145 | ||||
| chr22:41285984-41286065 | Common:1; Rare:22 | ||||
| chr22:41286164-41286557 | Common:2; Rare:122 | ||||
| chr22:41381846-41382019 | Common:3; Rare:73 | ||||
| chr22:41446778-41446980 | Rare:85 | ||||
| chr22:41468617-41468810 | Common:2; Rare:50 | ||||
| chr22:41468997-41469175 | Rare:67 | ||||
| chr22:41515270-41515497 | Rare:45; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:41560903-41561132 | Common:9; Rare:66 | ||||
| chr22:41620756-41620762 | Rare:1 |