| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67619689-67619988 | Common:1; Rare:87 | ||||
| chr14:67674584-67674971 | Common:1; Rare:98 | ||||
| chr14:67695717-67695841 | Rare:43 | ||||
| chr14:67816578-67816703 | Rare:22 | ||||
| chr14:69398245-69398387 | Rare:62 | ||||
| chr14:69398592-69398740 | Rare:36 | ||||
| chr14:69611456-69611708 | Common:1; Rare:86 | ||||
| chr14:70600635-70600942 | Common:3; Rare:73 | ||||
| chr14:71320296-71320476 | Rare:56 | ||||
| chr14:73058328-73058595 | Common:3; Rare:86 | ||||
| chr14:73458526-73458870 | Common:5; Rare:90 | ||||
| chr14:73644891-73645031 | Common:2; Rare:41; Clinvar:2 | ||||
| chr14:73851733-73851957 | Common:2; Rare:71 | ||||
| chr14:73886777-73886869 | Common:1; Rare:27 | ||||
| chr14:73950123-73950333 | Common:5; Rare:87; Clinvar (benign):3 |