| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45253480-45253546 | Common:2; Rare:29 | ||||
| chr14:49586286-49586782 | Common:1; Rare:249; Clinvar (benign):1 | ||||
| chr14:49586786-49586806 | Rare:7 | ||||
| chr14:49598670-49599038 | Common:2; Rare:141 | ||||
| chr14:49620561-49620835 | Common:2; Rare:113; Clinvar:3 | ||||
| chr14:49688182-49688266 | Rare:32 | ||||
| chr14:49767515-49767757 | Common:2; Rare:89 | ||||
| chr14:49767975-49768404 | Common:2; Rare:141 | ||||
| chr14:49777602-49777953 | Common:1; Rare:86 | ||||
| chr14:49795834-49796150 | Rare:61 | ||||
| chr14:49800737-49800868 | Rare:28 | ||||
| chr14:49892909-49893168 | Rare:105 | ||||
| chr14:50116536-50116695 | Rare:79 | ||||
| chr14:50312146-50312389 | Common:1; Rare:108 | ||||
| chr14:50396874-50396999 | Common:2; Rare:34 |