| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74019248-74019433 | Common:1; Rare:72 | ||||
| chr14:74493568-74493777 | Common:3; Rare:78; Clinvar (benign):4 | ||||
| chr14:74713065-74713200 | Rare:73 | ||||
| chr14:74763204-74763353 | Rare:47 | ||||
| chr14:74881837-74881964 | Rare:56 | ||||
| chr14:75002658-75002952 | Common:1; Rare:87; Clinvar:2 | ||||
| chr14:75127001-75127104 | Rare:30 | ||||
| chr14:75660825-75661314 | Common:4; Rare:119 | ||||
| chr14:77320849-77321051 | Rare:61; Clinvar:1 | ||||
| chr14:77377060-77377152 | Common:1; Rare:34 | ||||
| chr14:77457550-77457880 | Common:1; Rare:98 | ||||
| chr14:77708000-77708127 | Rare:63 | ||||
| chr14:81220834-81221066 | Common:1; Rare:111 | ||||
| chr14:81221279-81221471 | Common:1; Rare:48 | ||||
| chr14:88562901-88563085 | Rare:85 |