| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:36320383-36320404 | Rare:6 | ||||
| chr14:36320554-36320846 | Common:5; Rare:95 | ||||
| chr14:36520112-36520348 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:36661379-36661397 | Rare:3 | ||||
| chr14:36661740-36661934 | Rare:53; Clinvar:4 | ||||
| chr14:36662200-36662267 | Rare:18 | ||||
| chr14:37172001-37172730 | Common:6; Rare:265 | ||||
| chr14:37172732-37172783 | Rare:10 | ||||
| chr14:37197456-37197640 | Rare:34 | ||||
| chr14:37197718-37198112 | Common:3; Rare:127 | ||||
| chr14:37594186-37594495 | Rare:53 | ||||
| chr14:37594973-37595141 | Common:1; Rare:52 | ||||
| chr14:37595204-37595661 | Common:1; Rare:134 | ||||
| chr14:37595664-37595719 | Rare:10 | ||||
| chr14:37595779-37596038 | Common:2; Rare:53 |