| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73490820-73491073 | Common:5; Rare:99 | ||||
| chr14:73491198-73491260 | Rare:17 | ||||
| chr14:73491383-73491423 | Common:1; Rare:13 | ||||
| chr14:73491534-73491825 | Common:2; Rare:89 | ||||
| chr14:73569181-73569378 | Rare:73 | ||||
| chr14:73569719-73569926 | Common:5; Rare:93 | ||||
| chr14:73591630-73591952 | Common:1; Rare:74 | ||||
| chr14:73591977-73592226 | Common:2; Rare:104 | ||||
| chr14:73644762-73645045 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73713816-73713952 | Rare:41 | ||||
| chr14:73760033-73760594 | Common:4; Rare:104 | ||||
| chr14:73760639-73760777 | Common:1; Rare:24 | ||||
| chr14:73786703-73786924 | Rare:53 | ||||
| chr14:73787112-73787397 | Common:3; Rare:96 | ||||
| chr14:73787695-73787931 | Common:3; Rare:39 |