| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42070578-42070935 | Common:2; Rare:84; Clinvar:1 | ||||
| chr22:42074137-42074315 | Common:3; Rare:34 | ||||
| chr22:42090658-42090977 | Common:2; Rare:140; Clinvar (pathogenic):1 | ||||
| chr22:42614870-42615251 | Common:3; Rare:155 | ||||
| chr22:42649322-42649491 | Common:1; Rare:70 | ||||
| chr22:42720813-42720941 | Rare:40 | ||||
| chr22:42959860-42959926 | Rare:9 | ||||
| chr22:43015069-43015384 | Common:2; Rare:127 | ||||
| chr22:43089338-43089496 | Common:3; Rare:50 | ||||
| chr22:43151389-43151598 | Common:2; Rare:45 | ||||
| chr22:43955303-43955569 | Common:3; Rare:81 | ||||
| chr22:44024201-44024351 | Common:1; Rare:57 | ||||
| chr22:45163743-45164008 | Common:3; Rare:102 | ||||
| chr22:45212355-45212682 | Common:3; Rare:89 | ||||
| chr22:45309671-45309970 | Common:1; Rare:123 |