| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49586347-49586761 | Common:1; Rare:220 | ||||
| chr14:49598731-49598996 | Rare:98 | ||||
| chr14:49620564-49620827 | Common:2; Rare:107; Clinvar:3 | ||||
| chr14:49780659-49780761 | Rare:20 | ||||
| chr14:50312121-50312349 | Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:50944405-50944540 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51240102-51240287 | Common:1; Rare:75 | ||||
| chr14:51651627-51651968 | Common:4; Rare:95 | ||||
| chr14:51999502-51999796 | Common:1; Rare:58 | ||||
| chr14:52068994-52069215 | Common:2; Rare:52 | ||||
| chr14:52267613-52267727 | Common:2; Rare:40 | ||||
| chr14:52707051-52707226 | Common:1; Rare:76 | ||||
| chr14:52791453-52791757 | Common:1; Rare:106 | ||||
| chr14:55027073-55027290 | Common:2; Rare:59 | ||||
| chr14:55051470-55051749 | Rare:123 |