| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63641489-63641580 | Rare:18 | ||||
| chr14:63641802-63642196 | Common:7; Rare:124 | ||||
| chr14:63852869-63853071 | Common:1; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:64338040-64338215 | Common:1; Rare:43 | ||||
| chr14:64338535-64338785 | Common:4; Rare:59 | ||||
| chr14:64387795-64388391 | Common:2; Rare:181 | ||||
| chr14:64465350-64465585 | Common:1; Rare:64 | ||||
| chr14:64503602-64503972 | Common:3; Rare:150 | ||||
| chr14:64504543-64504828 | Rare:85 | ||||
| chr14:64914284-64914513 | Common:1; Rare:90 | ||||
| chr14:64987088-64987255 | Rare:65 | ||||
| chr14:65102464-65102876 | Common:7; Rare:109; Clinvar:1 | ||||
| chr14:65411712-65411921 | Common:2; Rare:55 | ||||
| chr14:65412547-65413034 | Common:6; Rare:149 | ||||
| chr14:66507767-66508171 | Rare:164 |