| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:76961620-76961940 | Common:6; Rare:90 | ||||
| chr14:76961860-76962390 | Common:1; Rare:180 | ||||
| chr14:76976160-76976662 | Common:2; Rare:115 | ||||
| chr14:76987991-76988426 | Common:7; Rare:132 | ||||
| chr14:77007350-77007637 | Common:3; Rare:148 | ||||
| chr14:77007730-77008500 | Common:7; Rare:265 | ||||
| chr14:77008897-77009350 | Common:12; Rare:114 | ||||
| chr14:77014277-77014522 | Common:3; Rare:44 | ||||
| chr14:77023430-77023720 | Common:4; Rare:118 | ||||
| chr14:77026603-77027595 | Common:37; Rare:841; Clinvar (pathogenic):2 | ||||
| chr14:77027592-77028194 | Common:1; Rare:526 | ||||
| chr14:77032859-77032982 | Common:2; Rare:25 | ||||
| chr14:77033155-77033960 | Common:32; Rare:410 | ||||
| chr14:77033956-77034135 | Rare:71 | ||||
| chr14:77034156-77034456 | Rare:94 |