| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:51651338-51651537 | Common:2; Rare:62 | ||||
| chr14:51651546-51651990 | Common:4; Rare:121 | ||||
| chr14:51847222-51847661 | Common:4; Rare:81 | ||||
| chr14:51860467-51860751 | Rare:73 | ||||
| chr14:51989277-51989704 | Common:2; Rare:128 | ||||
| chr14:51989757-51989857 | Rare:27 | ||||
| chr14:52552412-52552915 | Common:2; Rare:157 | ||||
| chr14:52553029-52553301 | Common:3; Rare:100 | ||||
| chr14:52695396-52695947 | Common:1; Rare:166 | ||||
| chr14:52706952-52707286 | Common:3; Rare:128 | ||||
| chr14:52729815-52730315 | Common:2; Rare:152 | ||||
| chr14:52791423-52791825 | Common:2; Rare:128 | ||||
| chr14:53150058-53150200 | Common:1; Rare:32 | ||||
| chr14:53152325-53152575 | Rare:101; Clinvar (benign):1 | ||||
| chr14:53152985-53153623 | Common:4; Rare:213; Clinvar:1; Clinvar (benign):1 |