| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67694787-67695065 | Rare:41 | ||||
| chr14:67941131-67941531 | Common:4; Rare:90 | ||||
| chr14:68089213-68089364 | Rare:21 | ||||
| chr14:68089409-68089559 | Common:1; Rare:31 | ||||
| chr14:68137832-68138001 | Rare:26 | ||||
| chr14:68172650-68172920 | Common:2; Rare:48 | ||||
| chr14:68181722-68181855 | Common:1; Rare:18 | ||||
| chr14:68232797-68232920 | Common:1; Rare:18 | ||||
| chr14:68291770-68292170 | Common:4; Rare:94; Clinvar (benign):1 | ||||
| chr14:68295340-68295750 | Common:1; Rare:63 | ||||
| chr14:68360180-68360750 | Common:5; Rare:92 | ||||
| chr14:68464630-68465050 | Common:2; Rare:64 | ||||
| chr14:68466470-68467080 | Common:4; Rare:87 | ||||
| chr14:68520900-68521300 | Common:1; Rare:69 | ||||
| chr14:68544280-68544550 | Common:2; Rare:42 |