| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104724606-104724747 | Common:1; Rare:30 | ||||
| chr14:104752995-104753212 | Common:2; Rare:80 | ||||
| chr14:104775702-104775958 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:105419729-105420032 | Rare:97 | ||||
| chr14:105468937-105469142 | Common:1; Rare:57 | ||||
| chr14:105469239-105469294 | Rare:7 | ||||
| chr14:105472748-105473057 | Common:3; Rare:55 | ||||
| chr14:105487032-105487226 | Common:1; Rare:57 | ||||
| chr15:23039529-23039687 | Common:1; Rare:71 | ||||
| chr15:23687231-23687446 | Common:1; Rare:79 | ||||
| chr15:25438984-25439266 | Common:2; Rare:113 | ||||
| chr15:29822246-29822623 | Common:2; Rare:142 | ||||
| chr15:30624122-30624374 | Common:2; Rare:37 | ||||
| chr15:30903788-30903970 | Rare:46 | ||||
| chr15:30991525-30991949 | Common:5; Rare:150 |