| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75464653-75464768 | Common:1; Rare:35 | ||||
| chr16:75555257-75555466 | Common:6; Rare:83 | ||||
| chr16:75556202-75556418 | Common:3; Rare:139; Clinvar (benign):7 | ||||
| chr16:75566273-75566438 | Rare:89 | ||||
| chr16:75623164-75623455 | Common:8; Rare:184 | ||||
| chr16:75647611-75647898 | Common:8; Rare:276; Clinvar:8; Clinvar (pathogenic):2 | ||||
| chr16:75648605-75648832 | Rare:99 | ||||
| chr16:77190671-77191015 | Common:22; Rare:217 | ||||
| chr16:77191123-77191236 | Common:2; Rare:95 | ||||
| chr16:77722282-77722618 | Common:4; Rare:118 | ||||
| chr16:78099259-78099873 | Common:6; Rare:395; Clinvar:3; Clinvar (benign):7 | ||||
| chr16:80540400-80540720 | Common:1; Rare:171 | ||||
| chr16:80540770-80541170 | Common:7; Rare:216 | ||||
| chr16:80803850-80804182 | Common:4; Rare:167 | ||||
| chr16:80804193-80804700 | Common:6; Rare:253 |