| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22598201-22598329 | Rare:45 | ||||
| chr14:22766537-22766925 | Common:2; Rare:185 | ||||
| chr14:22775520-22775590 | Rare:23; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:22780178-22780502 | Common:2; Rare:63 | ||||
| chr14:22815740-22815909 | Rare:34; Clinvar (benign):1 | ||||
| chr14:22819740-22819865 | Common:3; Rare:24; Clinvar (benign):1 | ||||
| chr14:22829741-22829943 | Common:1; Rare:65 | ||||
| chr14:22836363-22836665 | Common:4; Rare:67 | ||||
| chr14:22836667-22836698 | Common:1; Rare:6 | ||||
| chr14:22871248-22871443 | Common:2; Rare:36 | ||||
| chr14:22871647-22872009 | Rare:93 | ||||
| chr14:22872030-22872309 | Common:2; Rare:66 | ||||
| chr14:22876698-22877041 | Common:2; Rare:105 | ||||
| chr14:22919034-22919462 | Common:8; Rare:117 | ||||
| chr14:22929341-22929613 | Rare:68 |