| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58466851-58467120 | Common:1; Rare:85 | ||||
| chr19:58475930-58476380 | Common:7; Rare:260 | ||||
| chr19:58476668-58477118 | Common:2; Rare:232 | ||||
| chr19:58499150-58499582 | Common:7; Rare:254; Clinvar:10; Clinvar (benign):3 | ||||
| chr19:58511930-58512290 | Rare:121; Clinvar:1 | ||||
| chr19:58519754-58520054 | Rare:159 | ||||
| chr19:58543967-58544124 | Rare:73 | ||||
| chr19:58544163-58544756 | Common:7; Rare:392 | ||||
| chr19:58558486-58558723 | Rare:131 | ||||
| chr19:58558831-58559228 | Common:4; Rare:232 | ||||
| chr19:58572920-58573240 | Common:1; Rare:181 | ||||
| chr19:58573358-58573597 | Common:1; Rare:85 | ||||
| chr2:249340-249750 | Common:6; Rare:144 | ||||
| chr2:249750-250150 | Common:2; Rare:172 | ||||
| chr2:264747-265129 | Common:2; Rare:181 |