| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20455039-20455287 | Common:2; Rare:74 | ||||
| chr14:20683908-20684359 | Common:20; Rare:189; Clinvar:2; Clinvar (benign):4 | ||||
| chr14:20684418-20684756 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:20802788-20802970 | Common:1; Rare:24 | ||||
| chr14:21019636-21019951 | Common:3; Rare:80 | ||||
| chr14:21025015-21025212 | Rare:71 | ||||
| chr14:21025682-21026058 | Common:2; Rare:64 | ||||
| chr14:21070155-21070375 | Common:1; Rare:61 | ||||
| chr14:21437213-21437391 | Common:3; Rare:77 | ||||
| chr14:21476611-21476708 | Rare:49 | ||||
| chr14:21476863-21477271 | Common:2; Rare:135 | ||||
| chr14:21511277-21511495 | Rare:60 | ||||
| chr14:22589134-22589520 | Common:4; Rare:118 | ||||
| chr14:22598220-22598316 | Rare:30 | ||||
| chr14:22766518-22766727 | Common:1; Rare:114 |