| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69879232-69879417 | Common:3; Rare:41 | ||||
| chr14:70416938-70417124 | Rare:60 | ||||
| chr14:70600633-70600942 | Common:3; Rare:73 | ||||
| chr14:71320306-71320552 | Rare:74 | ||||
| chr14:72894063-72894260 | Common:4; Rare:67 | ||||
| chr14:73058328-73058595 | Common:3; Rare:86 | ||||
| chr14:73463607-73463807 | Common:1; Rare:32 | ||||
| chr14:73536961-73537336 | Common:6; Rare:34 | ||||
| chr14:73567838-73568128 | Common:1; Rare:73 | ||||
| chr14:73569051-73569292 | Rare:57 | ||||
| chr14:73592086-73592170 | Common:1; Rare:34 | ||||
| chr14:73610848-73610940 | Common:1; Rare:9 | ||||
| chr14:73644901-73645037 | Common:2; Rare:36; Clinvar:2 | ||||
| chr14:73787166-73787372 | Common:2; Rare:76 | ||||
| chr14:73950062-73950351 | Common:6; Rare:133; Clinvar (benign):4 |