| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31561089-31561433 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:32075670-32075954 | Common:1; Rare:54 | ||||
| chr14:32076611-32077053 | Common:3; Rare:126 | ||||
| chr14:32154358-32154713 | Common:2; Rare:68 | ||||
| chr14:32939443-32939582 | Common:2; Rare:22 | ||||
| chr14:34462215-34462575 | Common:1; Rare:126 | ||||
| chr14:34629907-34629993 | Rare:30 | ||||
| chr14:34874868-34874991 | Common:1; Rare:42 | ||||
| chr14:34875229-34875646 | Common:1; Rare:135 | ||||
| chr14:34982430-34982709 | Common:1; Rare:118 | ||||
| chr14:35018746-35019036 | Rare:49 | ||||
| chr14:35046089-35046707 | Common:3; Rare:218 | ||||
| chr14:35099326-35099599 | Common:1; Rare:41 | ||||
| chr14:35121707-35121866 | Rare:41 | ||||
| chr14:35122062-35122375 | Common:1; Rare:75 |