| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75278376-75278546 | Rare:34 | ||||
| chr14:75279060-75279123 | Rare:18 | ||||
| chr14:75427408-75427759 | Rare:79 | ||||
| chr14:75578389-75578706 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr14:75579516-75579669 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:75660813-75661494 | Common:7; Rare:174 | ||||
| chr14:77320824-77321104 | Rare:87; Clinvar:2 | ||||
| chr14:77377053-77377411 | Common:2; Rare:104 | ||||
| chr14:77457536-77457880 | Common:1; Rare:104 | ||||
| chr14:77616534-77616873 | Common:2; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr14:77707999-77708118 | Rare:56 | ||||
| chr14:77737036-77737294 | Common:2; Rare:47 | ||||
| chr14:81220867-81221054 | Common:1; Rare:88 | ||||
| chr14:81221279-81221456 | Common:1; Rare:44 | ||||
| chr14:81324124-81324309 | Common:1; Rare:28 |