| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30356770-30357016 | Common:1; Rare:81 | ||||
| chr22:30607038-30607201 | Common:3; Rare:46; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:31107402-31107667 | Common:2; Rare:84 | ||||
| chr22:31159996-31160273 | Common:2; Rare:95 | ||||
| chr22:31212104-31212345 | Rare:82 | ||||
| chr22:31290717-31290906 | Rare:77 | ||||
| chr22:31292425-31292677 | Common:1; Rare:50 | ||||
| chr22:31346549-31346762 | Common:6; Rare:39 | ||||
| chr22:31399442-31399660 | Rare:62 | ||||
| chr22:31489931-31490151 | Common:3; Rare:91 | ||||
| chr22:31496394-31496592 | Common:2; Rare:58 | ||||
| chr22:31630803-31631013 | Common:5; Rare:55 | ||||
| chr22:31753886-31754107 | Common:1; Rare:79 | ||||
| chr22:32202510-32202894 | Common:5; Rare:72 | ||||
| chr22:32355061-32355321 | Common:10; Rare:66 |