| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1249537-1249925 | Common:3; Rare:278 | ||||
| chr19:1251263-1251682 | Common:4; Rare:301 | ||||
| chr19:1253132-1253844 | Common:15; Rare:424 | ||||
| chr19:1275346-1275603 | Common:1; Rare:223 | ||||
| chr19:1275620-1276112 | Common:4; Rare:373 | ||||
| chr19:1354786-1355039 | Common:6; Rare:234 | ||||
| chr19:1401334-1401620 | Common:2; Rare:159; Clinvar:16; Clinvar (benign):14; Clinvar (pathogenic):3 | ||||
| chr19:1407229-1408125 | Common:7; Rare:564 | ||||
| chr19:1438144-1438465 | Common:2; Rare:214 | ||||
| chr19:1479153-1479345 | Common:2; Rare:138 | ||||
| chr19:1479504-1479652 | Common:2; Rare:69 | ||||
| chr19:1490275-1490474 | Common:8; Rare:140 | ||||
| chr19:1512960-1513121 | Common:2; Rare:83 | ||||
| chr19:1592293-1592516 | Rare:209 | ||||
| chr19:1592689-1592979 | Common:2; Rare:258 |