| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:66507638-66508222 | Common:1; Rare:226 | ||||
| chr14:66508883-66509129 | Common:1; Rare:79 | ||||
| chr14:66509192-66509271 | Rare:22 | ||||
| chr14:66509281-66509505 | Common:2; Rare:63 | ||||
| chr14:67240548-67240736 | Rare:23 | ||||
| chr14:67241008-67241722 | Common:6; Rare:181 | ||||
| chr14:67241835-67241960 | Common:1; Rare:25 | ||||
| chr14:67241975-67242036 | Rare:9 | ||||
| chr14:67359724-67360041 | Common:1; Rare:110 | ||||
| chr14:67360235-67360458 | Common:2; Rare:72 | ||||
| chr14:67488790-67488890 | Common:1; Rare:16 | ||||
| chr14:67514894-67514998 | Common:3; Rare:21 | ||||
| chr14:67600032-67600397 | Common:7; Rare:123; Clinvar (pathogenic):1 | ||||
| chr14:67619632-67619922 | Common:2; Rare:73 | ||||
| chr14:67674206-67674336 | Common:2; Rare:34 |