| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23307251-23307306 | Rare:10 | ||||
| chr14:23308364-23308456 | Rare:13 | ||||
| chr14:23320897-23321560 | Common:4; Rare:183; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr14:23321564-23321733 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:23321750-23321998 | Common:1; Rare:64 | ||||
| chr14:23322271-23322460 | Rare:42 | ||||
| chr14:23469200-23469459 | Common:3; Rare:86 | ||||
| chr14:23469501-23469781 | Common:1; Rare:82 | ||||
| chr14:23470055-23470130 | Common:1; Rare:34 | ||||
| chr14:23551727-23551922 | Rare:49 | ||||
| chr14:23555858-23556084 | Common:1; Rare:59 | ||||
| chr14:23556155-23556439 | Common:2; Rare:58 | ||||
| chr14:23566924-23567344 | Rare:95 | ||||
| chr14:23567534-23567643 | Rare:31 | ||||
| chr14:23567720-23567977 | Rare:51 |