| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73136291-73136569 | Common:4; Rare:86; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73136640-73136701 | Rare:13 | ||||
| chr14:73136707-73137081 | Common:2; Rare:83 | ||||
| chr14:73237401-73237545 | Common:1; Rare:30 | ||||
| chr14:73457488-73457699 | Common:2; Rare:45 | ||||
| chr14:73457918-73458199 | Common:6; Rare:66 | ||||
| chr14:73458210-73458328 | Common:1; Rare:23 | ||||
| chr14:73458453-73458904 | Common:6; Rare:121 | ||||
| chr14:73463465-73463654 | Common:2; Rare:42 | ||||
| chr14:73490766-73491258 | Common:6; Rare:161 | ||||
| chr14:73491332-73491684 | Common:2; Rare:103 | ||||
| chr14:73537025-73537361 | Common:2; Rare:28 | ||||
| chr14:73537784-73538095 | Common:4; Rare:49 | ||||
| chr14:73569009-73569094 | Rare:16 | ||||
| chr14:73569147-73569452 | Rare:109 |