| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:70416930-70417147 | Rare:68 | ||||
| chr14:70591912-70592040 | Common:2; Rare:25 | ||||
| chr14:70600642-70600923 | Common:3; Rare:63 | ||||
| chr14:70809754-70809969 | Common:1; Rare:52 | ||||
| chr14:70907348-70907616 | Common:3; Rare:105 | ||||
| chr14:71320308-71320488 | Rare:55 | ||||
| chr14:72926196-72926538 | Common:6; Rare:86 | ||||
| chr14:73027040-73027264 | Common:1; Rare:66 | ||||
| chr14:73058322-73058634 | Common:3; Rare:97 | ||||
| chr14:73237356-73237537 | Common:1; Rare:37 | ||||
| chr14:73297238-73297471 | Common:2; Rare:47 | ||||
| chr14:73568806-73569075 | Common:1; Rare:39 | ||||
| chr14:73644834-73645037 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73760012-73760217 | Common:1; Rare:34 | ||||
| chr14:73787116-73787325 | Common:1; Rare:77 |