| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77026777-77026787 | Rare:8 | ||||
| chr14:77027227-77027480 | Common:17; Rare:164; Clinvar (pathogenic):1 | ||||
| chr14:77027632-77027719 | Rare:29 | ||||
| chr14:77028012-77028115 | Rare:36 | ||||
| chr14:77032860-77033134 | Common:3; Rare:56 | ||||
| chr14:77033317-77033726 | Common:9; Rare:91 | ||||
| chr14:77034039-77034201 | Rare:37 | ||||
| chr14:77037147-77037465 | Common:3; Rare:53 | ||||
| chr14:77038454-77038486 | Rare:2 | ||||
| chr14:77038552-77038832 | Common:6; Rare:48 | ||||
| chr14:77039397-77039701 | Common:1; Rare:39 | ||||
| chr14:77040149-77040434 | Rare:47 | ||||
| chr14:77040436-77040705 | Rare:56 | ||||
| chr14:77040797-77041068 | Common:1; Rare:48 | ||||
| chr14:77041143-77041267 | Rare:26 |