| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1771465-1771853 | Common:3; Rare:154 | ||||
| chr16:1772612-1772893 | Common:3; Rare:94; Clinvar (pathogenic):2 | ||||
| chr16:1773088-1773215 | Rare:43 | ||||
| chr16:1773453-1773748 | Rare:127 | ||||
| chr16:1826757-1826982 | Common:3; Rare:73 | ||||
| chr16:1827179-1827538 | Common:2; Rare:190 | ||||
| chr16:1827713-1827769 | Rare:18 | ||||
| chr16:1943176-1943503 | Common:1; Rare:100 | ||||
| chr16:1964806-1965061 | Common:6; Rare:117 | ||||
| chr16:1971913-1972090 | Common:1; Rare:51 | ||||
| chr16:1976898-1977175 | Common:1; Rare:90 | ||||
| chr16:1984294-1984732 | Common:1; Rare:135; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr16:2047790-2048043 | Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2091194-2091564 | Common:19; Rare:160; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:2205683-2205763 | Common:2; Rare:35 |