| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75985686-75985798 | Rare:47; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:75986234-75986392 | Rare:32 | ||||
| chr14:77320854-77321064 | Rare:62; Clinvar:1 | ||||
| chr14:77376989-77377415 | Common:5; Rare:128 | ||||
| chr14:77457550-77457886 | Common:2; Rare:99 | ||||
| chr14:77457997-77458186 | Rare:50 | ||||
| chr14:77498795-77498949 | Rare:38 | ||||
| chr14:77616747-77617083 | Common:1; Rare:77; Clinvar (benign):2 | ||||
| chr14:77707991-77708131 | Common:1; Rare:71 | ||||
| chr14:77761114-77761368 | Common:2; Rare:80 | ||||
| chr14:81220867-81221054 | Common:1; Rare:88 | ||||
| chr14:81221264-81221474 | Common:1; Rare:51 | ||||
| chr14:81427399-81427673 | Common:3; Rare:64 | ||||
| chr14:81436414-81436625 | Common:3; Rare:80 | ||||
| chr14:81533782-81534123 | Rare:91 |