| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103057495-103057898 | Common:6; Rare:183 | ||||
| chr14:103333263-103333663 | Common:5; Rare:112 | ||||
| chr14:103333844-103334248 | Common:3; Rare:162 | ||||
| chr14:103334555-103335447 | Common:9; Rare:393 | ||||
| chr14:103385201-103385458 | Common:1; Rare:94 | ||||
| chr14:103522818-103523050 | Rare:70 | ||||
| chr14:103528989-103529264 | Common:1; Rare:78 | ||||
| chr14:103561697-103562110 | Common:11; Rare:239 | ||||
| chr14:103562626-103563044 | Common:8; Rare:162; Clinvar (benign):5 | ||||
| chr14:103629071-103629256 | Rare:90 | ||||
| chr14:103715397-103715854 | Common:1; Rare:157 | ||||
| chr14:103847569-103847758 | Common:3; Rare:82 | ||||
| chr14:103921480-103921758 | Common:3; Rare:81 | ||||
| chr14:104138400-104138628 | Common:1; Rare:78 | ||||
| chr14:104689481-104689634 | Rare:33 |