| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22766461-22766765 | Common:2; Rare:163 | ||||
| chr14:22767075-22767242 | Rare:53 | ||||
| chr14:22780189-22780432 | Common:2; Rare:48 | ||||
| chr14:22815790-22815980 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr14:22822819-22823057 | Common:2; Rare:55 | ||||
| chr14:22823242-22823302 | Common:1; Rare:12 | ||||
| chr14:22823571-22823694 | Rare:24 | ||||
| chr14:22829674-22829980 | Common:1; Rare:90 | ||||
| chr14:22836479-22836716 | Common:2; Rare:51 | ||||
| chr14:22837220-22837397 | Rare:62 | ||||
| chr14:22837507-22837614 | Rare:25 | ||||
| chr14:22837621-22837684 | Rare:13 | ||||
| chr14:22871463-22871509 | Rare:6 | ||||
| chr14:22872594-22872822 | Common:1; Rare:77 | ||||
| chr14:22919087-22919632 | Common:9; Rare:147 |