| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23387527-23387935 | Common:3; Rare:153; Clinvar:11; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr14:23389391-23389723 | Rare:108; Clinvar:17; Clinvar (benign):12 | ||||
| chr14:23392565-23393058 | Common:3; Rare:146; Clinvar:15; Clinvar (benign):9 | ||||
| chr14:23393339-23393923 | Common:3; Rare:148; Clinvar:14; Clinvar (benign):9 | ||||
| chr14:23396692-23397092 | Common:3; Rare:122; Clinvar:10; Clinvar (benign):9 | ||||
| chr14:23402441-23403039 | Common:4; Rare:171; Clinvar:11; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr14:23403238-23403326 | Rare:22 | ||||
| chr14:23405210-23405797 | Common:4; Rare:167; Clinvar:14; Clinvar (benign):13 | ||||
| chr14:23416248-23416496 | Common:1; Rare:65; Clinvar:9; Clinvar (benign):4 | ||||
| chr14:23442714-23443043 | Common:2; Rare:71 | ||||
| chr14:24132791-24132914 | Rare:35 | ||||
| chr14:28188494-28188636 | Common:4; Rare:61 | ||||
| chr14:28188816-28189007 | Common:6; Rare:48 | ||||
| chr14:30690232-30690470 | Common:2; Rare:8 | ||||
| chr14:32201685-32201857 | Rare:35 |