| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75464637-75464946 | Common:4; Rare:99 | ||||
| chr16:75494526-75494750 | Common:3; Rare:57 | ||||
| chr16:75494990-75495036 | Rare:11; Clinvar:1 | ||||
| chr16:75495361-75495474 | Rare:37 | ||||
| chr16:75555262-75555443 | Common:2; Rare:41 | ||||
| chr16:75555938-75555996 | Rare:20 | ||||
| chr16:75556123-75556437 | Common:3; Rare:117; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr16:75566172-75566425 | Common:2; Rare:113 | ||||
| chr16:75622765-75622908 | Common:1; Rare:39 | ||||
| chr16:75622920-75623048 | Common:2; Rare:36 | ||||
| chr16:75623091-75623584 | Common:8; Rare:167 | ||||
| chr16:75647426-75648008 | Common:5; Rare:247; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648040-75648413 | Rare:147 | ||||
| chr16:75648611-75648757 | Rare:62 | ||||
| chr16:77190637-77191249 | Common:15; Rare:217 |