| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67816553-67816751 | Rare:35; Clinvar:1 | ||||
| chr14:68796073-68796228 | Rare:62 | ||||
| chr14:68884166-68884442 | Rare:56 | ||||
| chr14:69191451-69191582 | Rare:25 | ||||
| chr14:69398239-69398937 | Common:2; Rare:192 | ||||
| chr14:69611478-69611755 | Common:1; Rare:95 | ||||
| chr14:69796814-69796874 | Rare:19; Clinvar:3 | ||||
| chr14:69796877-69796973 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:69796975-69797089 | Rare:39; Clinvar:7 | ||||
| chr14:69879232-69879449 | Common:4; Rare:62 | ||||
| chr14:70416955-70417348 | Common:2; Rare:97 | ||||
| chr14:71320306-71320552 | Rare:74 | ||||
| chr14:71321011-71321172 | Common:1; Rare:58 | ||||
| chr14:73058309-73058612 | Common:3; Rare:93 | ||||
| chr14:73458502-73458863 | Common:5; Rare:95 |