| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67600222-67600356 | Common:4; Rare:48 | ||||
| chr14:67619638-67619886 | Common:2; Rare:59 | ||||
| chr14:67816572-67816769 | Rare:36 | ||||
| chr14:68978974-68979441 | Common:3; Rare:126 | ||||
| chr14:69398253-69398426 | Common:1; Rare:67 | ||||
| chr14:69398582-69398739 | Rare:37 | ||||
| chr14:69611373-69611750 | Common:1; Rare:133 | ||||
| chr14:73058501-73058612 | Common:2; Rare:44 | ||||
| chr14:73567895-73568128 | Common:1; Rare:64 | ||||
| chr14:73569092-73569294 | Rare:49 | ||||
| chr14:73787166-73787372 | Common:2; Rare:76 | ||||
| chr14:73886785-73886897 | Common:2; Rare:38 | ||||
| chr14:73950107-73950351 | Common:5; Rare:107; Clinvar (benign):3 | ||||
| chr14:74019248-74019436 | Common:1; Rare:74 | ||||
| chr14:74084399-74084634 | Common:2; Rare:62 |