| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:29480705-29481132 | Common:3; Rare:172; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr22:29766947-29767495 | Common:5; Rare:171 | ||||
| chr22:29883015-29883232 | Common:1; Rare:56 | ||||
| chr22:30266845-30267059 | Rare:40 | ||||
| chr22:30289483-30289861 | Common:3; Rare:95 | ||||
| chr22:30326916-30327217 | Common:1; Rare:99 | ||||
| chr22:30356817-30357030 | Common:1; Rare:73 | ||||
| chr22:30425624-30425796 | Rare:43 | ||||
| chr22:30591842-30592177 | Common:5; Rare:103 | ||||
| chr22:30606979-30607227 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:31081124-31081341 | Common:1; Rare:56 | ||||
| chr22:31107480-31107717 | Common:2; Rare:77 | ||||
| chr22:31248176-31248358 | Common:1; Rare:39 | ||||
| chr22:31290718-31290906 | Rare:76 | ||||
| chr22:31292425-31292570 | Rare:32 |