| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69398232-69398426 | Common:1; Rare:79 | ||||
| chr14:69398644-69398740 | Rare:29 | ||||
| chr14:69611480-69611761 | Common:1; Rare:93 | ||||
| chr14:70416984-70417121 | Rare:44 | ||||
| chr14:73058269-73058602 | Common:3; Rare:110 | ||||
| chr14:73136342-73136525 | Common:4; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73458520-73458853 | Common:5; Rare:85 | ||||
| chr14:73569202-73569292 | Rare:28 | ||||
| chr14:73644893-73645031 | Common:2; Rare:40; Clinvar:2 | ||||
| chr14:73760257-73760409 | Common:1; Rare:33 | ||||
| chr14:73787125-73787365 | Common:2; Rare:85 | ||||
| chr14:73851849-73851932 | Rare:29 | ||||
| chr14:73886768-73886893 | Common:2; Rare:42 | ||||
| chr14:73950080-73950333 | Common:5; Rare:104; Clinvar (benign):3 | ||||
| chr14:74019233-74019411 | Common:1; Rare:71 |