| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39217304-39217641 | Common:2; Rare:66 | ||||
| chr14:39218285-39218525 | Rare:30 | ||||
| chr14:39219176-39219294 | Rare:26 | ||||
| chr14:39232784-39232988 | Common:1; Rare:43 | ||||
| chr14:44316945-44317160 | Common:1; Rare:50 | ||||
| chr14:45526980-45527340 | Common:3; Rare:63 | ||||
| chr14:45551252-45551502 | Common:5; Rare:82 | ||||
| chr14:48536400-48536700 | Common:1; Rare:62 | ||||
| chr14:48563541-48563762 | Common:1; Rare:41 | ||||
| chr14:49633938-49634113 | Common:1; Rare:80; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:49634210-49634528 | Common:1; Rare:146; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49853914-49854041 | Rare:15 | ||||
| chr14:49861657-49862057 | Common:2; Rare:169 | ||||
| chr14:49862108-49862307 | Rare:41 | ||||
| chr14:49862839-49863140 | Common:1; Rare:104 |