| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75002741-75002972 | Common:1; Rare:72; Clinvar:2 | ||||
| chr14:75063959-75064184 | Common:1; Rare:57 | ||||
| chr14:75069488-75069670 | Common:1; Rare:42 | ||||
| chr14:75127001-75127128 | Rare:42 | ||||
| chr14:75176566-75176727 | Rare:52 | ||||
| chr14:75660797-75661366 | Common:5; Rare:141 | ||||
| chr14:76151777-76151982 | Rare:71 | ||||
| chr14:76812833-76813018 | Common:1; Rare:67 | ||||
| chr14:77098001-77098399 | Rare:120 | ||||
| chr14:77376947-77377411 | Common:5; Rare:132 | ||||
| chr14:77457523-77457886 | Common:2; Rare:112 | ||||
| chr14:77457997-77458160 | Rare:47 | ||||
| chr14:77616582-77616710 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:77616755-77617114 | Common:1; Rare:82; Clinvar (benign):2 | ||||
| chr14:77707985-77708209 | Common:2; Rare:114 |