| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104171522-104171752 | Rare:58 | ||||
| chr14:104202096-104202305 | Common:3; Rare:37 | ||||
| chr14:104341999-104342399 | Common:10; Rare:199 | ||||
| chr14:104429340-104429600 | Common:3; Rare:78 | ||||
| chr14:104537272-104537603 | Common:3; Rare:57 | ||||
| chr14:104563980-104564280 | Common:5; Rare:54 | ||||
| chr14:104649953-104651128 | Common:9; Rare:455 | ||||
| chr14:104680889-104681544 | Common:9; Rare:207 | ||||
| chr14:104681784-104681918 | Common:2; Rare:28 | ||||
| chr14:104687790-104688159 | Common:3; Rare:175 | ||||
| chr14:104688112-104688396 | Rare:117 | ||||
| chr14:104792501-104793001 | Common:4; Rare:229; Clinvar:4; Clinvar (benign):4 | ||||
| chr14:104797431-104797576 | Rare:20 | ||||
| chr14:104806102-104806698 | Common:25; Rare:157 | ||||
| chr14:104815807-104816489 | Common:7; Rare:476 |