| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:68793041-68793363 | Common:1; Rare:71 | ||||
| chr14:69191428-69191572 | Rare:31 | ||||
| chr14:69260004-69260206 | Common:2; Rare:56 | ||||
| chr14:69398248-69398387 | Rare:61 | ||||
| chr14:69398595-69398747 | Rare:36 | ||||
| chr14:69611458-69611750 | Common:1; Rare:100 | ||||
| chr14:69767687-69767911 | Common:1; Rare:99 | ||||
| chr14:70416973-70417115 | Rare:47 | ||||
| chr14:71320308-71320491 | Rare:57 | ||||
| chr14:72926188-72926516 | Common:6; Rare:79 | ||||
| chr14:73058302-73058579 | Common:3; Rare:82 | ||||
| chr14:73458504-73458878 | Common:5; Rare:97 | ||||
| chr14:73644883-73645034 | Common:3; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73714325-73714516 | Common:2; Rare:71 | ||||
| chr14:73787181-73787351 | Common:2; Rare:68 |