| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67674576-67674933 | Common:1; Rare:90 | ||||
| chr14:67816578-67816732 | Rare:27 | ||||
| chr14:67819672-67819831 | Rare:40 | ||||
| chr14:69191411-69191548 | Rare:27 | ||||
| chr14:69259844-69260166 | Common:3; Rare:75 | ||||
| chr14:69398251-69398746 | Common:2; Rare:146 | ||||
| chr14:69611462-69611708 | Common:1; Rare:83 | ||||
| chr14:69767702-69767953 | Common:1; Rare:98 | ||||
| chr14:70417025-70417124 | Rare:25 | ||||
| chr14:70809778-70809897 | Common:1; Rare:25 | ||||
| chr14:73058301-73058587 | Common:3; Rare:87 | ||||
| chr14:73136361-73136555 | Common:4; Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73568981-73569292 | Rare:67 | ||||
| chr14:73644900-73645037 | Common:2; Rare:37; Clinvar:2 | ||||
| chr14:73714353-73714499 | Common:1; Rare:52 |