| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75126992-75127349 | Common:4; Rare:101 | ||||
| chr14:75176862-75177017 | Rare:36 | ||||
| chr14:75427615-75428127 | Rare:198 | ||||
| chr14:75578337-75578676 | Common:2; Rare:65; Clinvar (benign):1 | ||||
| chr14:75578694-75579094 | Common:7; Rare:127; Clinvar:3; Clinvar (benign):7 | ||||
| chr14:75660800-75661057 | Rare:66 | ||||
| chr14:75661206-75661337 | Common:2; Rare:35 | ||||
| chr14:75661415-75661565 | Common:2; Rare:62 | ||||
| chr14:75985697-75985832 | Rare:68; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr14:76151728-76151988 | Rare:97 | ||||
| chr14:76375875-76376275 | Common:6; Rare:74 | ||||
| chr14:76812822-76813023 | Common:2; Rare:79 | ||||
| chr14:77028628-77028916 | Rare:96 | ||||
| chr14:77097788-77098348 | Common:1; Rare:174 | ||||
| chr14:77141275-77142033 | Common:4; Rare:158 |