| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20413289-20413390 | Common:1; Rare:10 | ||||
| chr14:20413399-20413632 | Common:4; Rare:63 | ||||
| chr14:20413832-20414034 | Rare:41 | ||||
| chr14:20454488-20454722 | Rare:83 | ||||
| chr14:20454732-20455324 | Common:7; Rare:156 | ||||
| chr14:20455348-20455689 | Rare:94 | ||||
| chr14:20461017-20461220 | Common:1; Rare:66 | ||||
| chr14:20461326-20461679 | Common:1; Rare:105 | ||||
| chr14:20461814-20462038 | Common:2; Rare:54 | ||||
| chr14:20469316-20469807 | Common:1; Rare:136; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:20469907-20470230 | Common:1; Rare:47 | ||||
| chr14:20470256-20470290 | Common:1; Rare:2 | ||||
| chr14:20470665-20470762 | Rare:18 | ||||
| chr14:20609401-20609711 | Common:6; Rare:86 | ||||
| chr14:20609900-20610179 | Common:3; Rare:105 |