| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31208146-31208180 | Rare:6 | ||||
| chr14:31420490-31420854 | Common:5; Rare:113 | ||||
| chr14:31457314-31457577 | Common:2; Rare:96 | ||||
| chr14:31561089-31561491 | Common:4; Rare:111; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076021-32076326 | Common:2; Rare:80 | ||||
| chr14:32076563-32077071 | Common:3; Rare:140 | ||||
| chr14:32077169-32077368 | Common:1; Rare:42 | ||||
| chr14:34462194-34462558 | Common:1; Rare:132 | ||||
| chr14:34539629-34539888 | Common:1; Rare:70 | ||||
| chr14:34630060-34630262 | Common:5; Rare:97 | ||||
| chr14:34714538-34714763 | Common:3; Rare:82 | ||||
| chr14:34875234-34875462 | Rare:90 | ||||
| chr14:34982372-34982690 | Common:1; Rare:125 | ||||
| chr14:35046053-35046611 | Common:2; Rare:188 | ||||
| chr14:35046621-35046715 | Common:2; Rare:36 |