| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:70416914-70417112 | Rare:65 | ||||
| chr14:71320308-71320487 | Rare:54 | ||||
| chr14:73058341-73058595 | Common:3; Rare:82 | ||||
| chr14:73569136-73569292 | Rare:43 | ||||
| chr14:73787166-73787386 | Common:2; Rare:79 | ||||
| chr14:73886785-73886869 | Common:1; Rare:25 | ||||
| chr14:73950035-73950348 | Common:6; Rare:139; Clinvar (benign):5 | ||||
| chr14:73961542-73961752 | Common:4; Rare:42; Clinvar (benign):3 | ||||
| chr14:74019263-74019436 | Common:1; Rare:68 | ||||
| chr14:74084397-74084737 | Common:7; Rare:83 | ||||
| chr14:74493261-74493776 | Common:4; Rare:164; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74612233-74612435 | Rare:35 | ||||
| chr14:74713057-74713207 | Rare:81 | ||||
| chr14:75069478-75069732 | Common:1; Rare:62 | ||||
| chr14:75126945-75127128 | Rare:64 |