| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74700791-74700983 | Common:2; Rare:42 | ||||
| chr16:74701131-74701351 | Common:1; Rare:48 | ||||
| chr16:75433348-75433812 | Common:4; Rare:150 | ||||
| chr16:75464352-75464459 | Common:4; Rare:47 | ||||
| chr16:75647605-75647788 | Common:1; Rare:92; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190706-77190997 | Common:10; Rare:93 | ||||
| chr16:77191086-77191221 | Common:2; Rare:57 | ||||
| chr16:77722284-77722541 | Common:4; Rare:73 | ||||
| chr16:79600732-79600958 | Common:1; Rare:65 | ||||
| chr16:81006367-81006553 | Common:1; Rare:42 | ||||
| chr16:81006825-81007272 | Common:3; Rare:150 | ||||
| chr16:81077213-81077319 | Common:1; Rare:47 | ||||
| chr16:82170164-82170286 | Common:3; Rare:66 | ||||
| chr16:84116806-84117078 | Common:3; Rare:108 | ||||
| chr16:84145104-84145292 | Common:1; Rare:92; Clinvar:1 |