| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50230740-50231255 | Common:12; Rare:297; Clinvar (benign):3 | ||||
| chr14:50231505-50231804 | Common:4; Rare:277 | ||||
| chr14:50231819-50232219 | Common:5; Rare:526 | ||||
| chr14:50312077-50312477 | Common:5; Rare:722; Clinvar:3; Clinvar (benign):3 | ||||
| chr14:50312528-50312740 | Common:14; Rare:128 | ||||
| chr14:50321033-50321456 | Rare:185 | ||||
| chr14:50342744-50342863 | Common:1; Rare:25 | ||||
| chr14:50396020-50396897 | Common:27; Rare:424 | ||||
| chr14:50396832-50397043 | Common:7; Rare:203 | ||||
| chr14:50397070-50397710 | Common:4; Rare:383 | ||||
| chr14:50531528-50531745 | Common:1; Rare:36 | ||||
| chr14:50531743-50532425 | Common:6; Rare:366 | ||||
| chr14:50532399-50532909 | Common:17; Rare:439 | ||||
| chr14:50665177-50665577 | Rare:223 | ||||
| chr14:50667627-50668027 | Rare:215 |