| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74606659-74607206 | Common:1; Rare:256 | ||||
| chr16:74666794-74667096 | Common:5; Rare:114 | ||||
| chr16:74985087-74985316 | Common:2; Rare:72 | ||||
| chr16:75148937-75149067 | Common:1; Rare:54 | ||||
| chr16:75251504-75251825 | Common:1; Rare:114 | ||||
| chr16:75433288-75433958 | Common:5; Rare:224 | ||||
| chr16:75464342-75464445 | Common:4; Rare:43 | ||||
| chr16:75464631-75464827 | Common:1; Rare:69 | ||||
| chr16:75495392-75495555 | Common:2; Rare:60 | ||||
| chr16:75555978-75555990 | Rare:4 | ||||
| chr16:75556021-75556369 | Common:3; Rare:133; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr16:75566242-75566628 | Common:3; Rare:177 | ||||
| chr16:75623200-75623352 | Common:3; Rare:58 | ||||
| chr16:75647605-75647867 | Common:4; Rare:132; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648207-75648343 | Rare:43 |