| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74881715-74882009 | Common:1; Rare:120 | ||||
| chr14:75002559-75003026 | Common:1; Rare:147; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75051137-75051234 | Rare:29 | ||||
| chr14:75051367-75051526 | Common:2; Rare:40; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75063632-75063757 | Rare:21 | ||||
| chr14:75063954-75064218 | Common:1; Rare:74 | ||||
| chr14:75069190-75069351 | Common:2; Rare:68 | ||||
| chr14:75069380-75069689 | Common:2; Rare:76 | ||||
| chr14:75126692-75127216 | Common:4; Rare:161 | ||||
| chr14:75175877-75176040 | Common:1; Rare:26 | ||||
| chr14:75176081-75176282 | Common:1; Rare:42 | ||||
| chr14:75176550-75176652 | Rare:48 | ||||
| chr14:75176919-75177089 | Rare:38 | ||||
| chr14:75427662-75427965 | Rare:65 | ||||
| chr14:75522249-75522573 | Rare:60 |