| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:76978013-76978325 | Common:3; Rare:75 | ||||
| chr14:77000080-77000750 | Common:1; Rare:155 | ||||
| chr14:77000757-77001157 | Common:2; Rare:84 | ||||
| chr14:77022334-77022496 | Rare:32 | ||||
| chr14:77022943-77023434 | Common:4; Rare:180 | ||||
| chr14:77023354-77023559 | Common:3; Rare:88 | ||||
| chr14:77023907-77024625 | Common:9; Rare:341 | ||||
| chr14:77027088-77027488 | Common:20; Rare:304; Clinvar (pathogenic):1 | ||||
| chr14:77027685-77028155 | Common:1; Rare:450 | ||||
| chr14:77032107-77032624 | Common:5; Rare:230 | ||||
| chr14:77032795-77033226 | Common:6; Rare:158 | ||||
| chr14:77033182-77033529 | Common:23; Rare:158 | ||||
| chr14:77033453-77033730 | Common:10; Rare:152 | ||||
| chr14:77033912-77034340 | Rare:175 | ||||
| chr14:77036470-77036960 | Common:2; Rare:114 |