| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20684427-20684686 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:21025682-21025963 | Common:2; Rare:50 | ||||
| chr14:21383931-21384053 | Common:1; Rare:51 | ||||
| chr14:21456047-21456470 | Common:3; Rare:108 | ||||
| chr14:21476849-21477267 | Common:2; Rare:138 | ||||
| chr14:21511300-21511522 | Rare:56 | ||||
| chr14:22589144-22589476 | Common:4; Rare:107 | ||||
| chr14:22766554-22766699 | Common:1; Rare:77 | ||||
| chr14:22929354-22929609 | Rare:58 | ||||
| chr14:22982594-22982916 | Common:2; Rare:109 | ||||
| chr14:23010119-23010268 | Rare:48 | ||||
| chr14:23034870-23035215 | Common:2; Rare:72 | ||||
| chr14:23095102-23095567 | Common:3; Rare:210 | ||||
| chr14:23306730-23306867 | Common:1; Rare:32 | ||||
| chr14:23555938-23556334 | Common:4; Rare:104 |