| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:20900756-20900819 | Rare:22 | ||||
| chr16:20900823-20900873 | Rare:13 | ||||
| chr16:22436942-22437061 | Rare:43 | ||||
| chr16:23557336-23557629 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641229-23641523 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:25111490-25111796 | Common:2; Rare:81 | ||||
| chr16:27268719-27268891 | Common:1; Rare:62 | ||||
| chr16:27549892-27550158 | Common:2; Rare:93 | ||||
| chr16:28846256-28846656 | Common:2; Rare:134; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:28974665-28974792 | Rare:57 | ||||
| chr16:29995589-29995698 | Common:1; Rare:53 | ||||
| chr16:29996086-29996266 | Common:2; Rare:64 | ||||
| chr16:30065456-30065889 | Rare:140 | ||||
| chr16:30069548-30069943 | Common:1; Rare:147; Clinvar:5; Clinvar (benign):6 | ||||
| chr16:30075905-30076040 | Rare:49 |