| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20683707-20684244 | Common:54; Rare:520; Clinvar:3; Clinvar (benign):3 | ||||
| chr14:20684299-20684728 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):7 | ||||
| chr14:20801508-20802126 | Rare:291 | ||||
| chr14:20802135-20802566 | Common:7; Rare:176 | ||||
| chr14:20802700-20803100 | Common:4; Rare:150 | ||||
| chr14:20803228-20803687 | Common:7; Rare:265 | ||||
| chr14:20989633-20990086 | Common:42; Rare:515 | ||||
| chr14:20990048-20990448 | Common:2; Rare:144 | ||||
| chr14:20990359-20990508 | Common:2; Rare:54 | ||||
| chr14:20990417-20990535 | Common:2; Rare:37 | ||||
| chr14:21024091-21024493 | Common:2; Rare:71 | ||||
| chr14:21024646-21025465 | Common:3; Rare:659 | ||||
| chr14:21025666-21026063 | Common:8; Rare:204 | ||||
| chr14:21070015-21070535 | Common:7; Rare:274 | ||||
| chr14:21098480-21099120 | Common:1; Rare:298 |