| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77321225-77321440 | Common:4; Rare:116 | ||||
| chr14:77377052-77377415 | Common:2; Rare:107 | ||||
| chr14:77457453-77457876 | Common:3; Rare:129 | ||||
| chr14:77457966-77458253 | Rare:68 | ||||
| chr14:77459410-77459639 | Rare:52 | ||||
| chr14:77616818-77617110 | Common:1; Rare:56 | ||||
| chr14:77707995-77708230 | Common:2; Rare:112 | ||||
| chr14:77799857-77800148 | Common:1; Rare:50 | ||||
| chr14:79279214-79279443 | Common:3; Rare:46 | ||||
| chr14:80941690-80941966 | Common:4; Rare:67 | ||||
| chr14:81220686-81221072 | Common:3; Rare:145 | ||||
| chr14:81221275-81221421 | Common:1; Rare:32 | ||||
| chr14:81436411-81436631 | Common:3; Rare:84 | ||||
| chr14:87992964-87993292 | Common:4; Rare:153; Clinvar:15; Clinvar (benign):8; Clinvar (pathogenic):8 | ||||
| chr14:88270879-88271002 | Common:1; Rare:20 |