| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73462108-73462524 | Common:2; Rare:94 | ||||
| chr14:73569928-73570041 | Common:2; Rare:82 | ||||
| chr14:73783290-73783600 | Common:2; Rare:68 | ||||
| chr14:74618630-74618970 | Common:3; Rare:103 | ||||
| chr14:74950830-74951270 | Common:1; Rare:90 | ||||
| chr14:76956370-76956670 | Common:6; Rare:62 | ||||
| chr14:77027090-77027570 | Common:20; Rare:293; Clinvar (pathogenic):1 | ||||
| chr14:77027810-77028070 | Rare:169 | ||||
| chr14:77499820-77500369 | Common:5; Rare:132 | ||||
| chr14:81170280-81170560 | Common:1; Rare:85 | ||||
| chr14:81219339-81219514 | Rare:69 | ||||
| chr14:86892500-86892810 | Rare:46 | ||||
| chr14:89368570-89369201 | Common:9; Rare:265 | ||||
| chr14:89910577-89911387 | Common:7; Rare:192 | ||||
| chr14:90383110-90383610 | Common:9; Rare:326 |