| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24114898-24115397 | Common:5; Rare:254 | ||||
| chr14:24135943-24136287 | Common:2; Rare:186 | ||||
| chr14:24141390-24141898 | Common:3; Rare:203 | ||||
| chr14:24146537-24146961 | Common:6; Rare:254 | ||||
| chr14:24147130-24147611 | Common:8; Rare:213 | ||||
| chr14:24147829-24148845 | Common:5; Rare:348 | ||||
| chr14:24195302-24195858 | Common:5; Rare:260 | ||||
| chr14:24213070-24213340 | Common:1; Rare:67 | ||||
| chr14:24213301-24213668 | Common:6; Rare:189 | ||||
| chr14:24231930-24232240 | Rare:120 | ||||
| chr14:24232291-24232712 | Common:16; Rare:195 | ||||
| chr14:24232714-24233010 | Common:2; Rare:125 | ||||
| chr14:24242256-24242446 | Common:1; Rare:116; Clinvar:2; Clinvar (benign):5 | ||||
| chr14:24242559-24242791 | Common:2; Rare:113; Clinvar:2; Clinvar (benign):4 | ||||
| chr14:24242940-24243180 | Common:3; Rare:78 |