| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:726848-727150 | Common:5; Rare:76 | ||||
| chr16:740942-741133 | Rare:67 | ||||
| chr16:1351860-1351974 | Common:1; Rare:53; Clinvar:5; Clinvar (benign):1 | ||||
| chr16:1474980-1475141 | Common:3; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:1493241-1493595 | Common:4; Rare:109 | ||||
| chr16:1706017-1706232 | Common:2; Rare:75 | ||||
| chr16:1771486-1771862 | Common:3; Rare:151 | ||||
| chr16:1773071-1773213 | Rare:46; Clinvar (pathogenic):1 | ||||
| chr16:1782508-1783012 | Common:4; Rare:166 | ||||
| chr16:1826777-1826968 | Common:3; Rare:58 | ||||
| chr16:1827168-1827229 | Common:1; Rare:29 | ||||
| chr16:1964805-1965016 | Common:6; Rare:96 | ||||
| chr16:2047737-2048024 | Rare:134; Clinvar:2 | ||||
| chr16:2267841-2267881 | Rare:15 | ||||
| chr16:2268059-2268186 | Common:1; Rare:66 |