| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77320276-77320435 | Common:2; Rare:43; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr14:77320818-77321094 | Rare:88; Clinvar:3 | ||||
| chr14:77377045-77377190 | Common:1; Rare:51 | ||||
| chr14:77377288-77377472 | Common:2; Rare:64 | ||||
| chr14:77457529-77457886 | Common:2; Rare:108 | ||||
| chr14:77457971-77458155 | Rare:54 | ||||
| chr14:77498789-77498951 | Rare:42 | ||||
| chr14:77707991-77708201 | Common:2; Rare:107 | ||||
| chr14:77761104-77761279 | Common:1; Rare:63 | ||||
| chr14:79279115-79279655 | Common:4; Rare:125 | ||||
| chr14:79279759-79279808 | Rare:4 | ||||
| chr14:79279868-79280069 | Rare:45 | ||||
| chr14:79280352-79280558 | Rare:54 | ||||
| chr14:79280713-79280854 | Rare:25 | ||||
| chr14:80941700-80941963 | Common:4; Rare:64 |