| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:61321487-61321737 | Common:3; Rare:63 | ||||
| chr14:63641839-63642162 | Common:4; Rare:106 | ||||
| chr14:63727993-63728144 | Common:2; Rare:71 | ||||
| chr14:64387937-64388413 | Common:2; Rare:165 | ||||
| chr14:64503601-64504193 | Common:4; Rare:211 | ||||
| chr14:64504568-64504895 | Common:1; Rare:98 | ||||
| chr14:64914302-64914493 | Common:1; Rare:79 | ||||
| chr14:65101637-65101777 | Rare:32 | ||||
| chr14:65102147-65102549 | Common:3; Rare:137; Clinvar:5; Clinvar (benign):10 | ||||
| chr14:65412544-65412811 | Common:2; Rare:82 | ||||
| chr14:66507813-66508159 | Rare:136 | ||||
| chr14:67359761-67360002 | Rare:75 | ||||
| chr14:67619667-67619923 | Common:2; Rare:61 | ||||
| chr14:67674082-67674355 | Common:2; Rare:67 | ||||
| chr14:67816578-67816720 | Rare:25 |