| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:58427628-58427749 | Rare:44 | ||||
| chr14:59484347-59484592 | Common:3; Rare:93 | ||||
| chr14:59919944-59920175 | Common:2; Rare:53 | ||||
| chr14:60091809-60092367 | Common:10; Rare:199 | ||||
| chr14:60249579-60249641 | Rare:19 | ||||
| chr14:60980987-60981280 | Rare:115 | ||||
| chr14:61695225-61695586 | Common:3; Rare:109 | ||||
| chr14:61762214-61762454 | Common:3; Rare:81 | ||||
| chr14:63204337-63204462 | Rare:23 | ||||
| chr14:63543332-63543613 | Common:3; Rare:79 | ||||
| chr14:63641490-63641703 | Common:2; Rare:58 | ||||
| chr14:63641823-63642162 | Common:4; Rare:112 | ||||
| chr14:63728018-63728144 | Common:1; Rare:63 | ||||
| chr14:63852826-63853079 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:64387930-64388413 | Common:2; Rare:165 |