| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1320184-1320464 | Common:2; Rare:84 | ||||
| chr16:1351852-1352003 | Common:1; Rare:82; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1420695-1421021 | Common:1; Rare:136 | ||||
| chr16:1474976-1475096 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:1493345-1493592 | Common:3; Rare:66 | ||||
| chr16:1612029-1612171 | Rare:44; Clinvar:1 | ||||
| chr16:1706030-1706263 | Common:2; Rare:75 | ||||
| chr16:1771445-1771848 | Common:3; Rare:162 | ||||
| chr16:1772384-1772844 | Common:4; Rare:186; Clinvar (pathogenic):2 | ||||
| chr16:1773092-1773219 | Rare:44 | ||||
| chr16:1773538-1773609 | Rare:26 | ||||
| chr16:1782495-1783050 | Common:4; Rare:194 | ||||
| chr16:1816894-1817188 | Common:2; Rare:139 | ||||
| chr16:1826786-1826968 | Common:3; Rare:54 | ||||
| chr16:1827161-1827238 | Common:1; Rare:36 |