| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:76151731-76152060 | Common:1; Rare:107 | ||||
| chr14:76152361-76152643 | Common:3; Rare:58 | ||||
| chr14:76812166-76812409 | Rare:44 | ||||
| chr14:76812455-76812667 | Common:2; Rare:42 | ||||
| chr14:76812677-76813038 | Common:4; Rare:135 | ||||
| chr14:77028367-77028562 | Common:3; Rare:53 | ||||
| chr14:77028573-77029021 | Common:1; Rare:140 | ||||
| chr14:77097514-77097694 | Common:1; Rare:42 | ||||
| chr14:77097718-77098476 | Common:1; Rare:217 | ||||
| chr14:77098635-77098711 | Rare:20 | ||||
| chr14:77098971-77099141 | Rare:30 | ||||
| chr14:77099478-77099613 | Rare:10 | ||||
| chr14:77181559-77181931 | Common:3; Rare:84 | ||||
| chr14:77320276-77320648 | Common:5; Rare:121; Clinvar:14; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr14:77320738-77321529 | Common:10; Rare:301; Clinvar:3; Clinvar (benign):3 |