| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67816583-67816712 | Rare:22 | ||||
| chr14:68793041-68793336 | Common:1; Rare:66 | ||||
| chr14:69398229-69398404 | Rare:72 | ||||
| chr14:69398576-69398714 | Rare:34 | ||||
| chr14:70416976-70417107 | Rare:43 | ||||
| chr14:73058328-73058583 | Common:3; Rare:78 | ||||
| chr14:73569218-73569286 | Rare:22 | ||||
| chr14:73950113-73950323 | Common:5; Rare:79; Clinvar (benign):3 | ||||
| chr14:74019265-74019450 | Common:1; Rare:70 | ||||
| chr14:74493252-74493553 | Common:1; Rare:81; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:74493568-74493777 | Common:3; Rare:78; Clinvar (benign):4 | ||||
| chr14:74713068-74713200 | Rare:71 | ||||
| chr14:75002741-75002967 | Common:1; Rare:68; Clinvar:2 | ||||
| chr14:75660834-75661037 | Rare:54 | ||||
| chr14:75661183-75661292 | Common:2; Rare:29 |