| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:60658271-60658511 | Rare:51 | ||||
| chr14:60723141-60723217 | Common:1; Rare:25 | ||||
| chr14:60980966-60981323 | Common:1; Rare:136 | ||||
| chr14:61527865-61527980 | Common:2; Rare:22 | ||||
| chr14:61695745-61695833 | Rare:32 | ||||
| chr14:61762181-61762426 | Common:4; Rare:72 | ||||
| chr14:63543325-63543594 | Common:3; Rare:73 | ||||
| chr14:63641789-63642172 | Common:6; Rare:123 | ||||
| chr14:63727926-63728172 | Common:3; Rare:102 | ||||
| chr14:64387929-64388457 | Common:2; Rare:179 | ||||
| chr14:64465342-64465595 | Common:1; Rare:68 | ||||
| chr14:64503582-64504047 | Common:3; Rare:173 | ||||
| chr14:64504568-64504894 | Common:1; Rare:98 | ||||
| chr14:64914195-64914532 | Common:3; Rare:117 | ||||
| chr14:65102281-65102577 | Common:2; Rare:97; Clinvar:5; Clinvar (benign):10 |