| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28711260-28711550 | |||||
| chr16:28822340-28822791 | Common:2; Rare:435 | ||||
| chr16:28822810-28824670 | Common:67; Rare:2804 | ||||
| chr16:28844246-28844473 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28844381-28845737 | Common:18; Rare:976; Clinvar:6; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr16:28846210-28846796 | Common:14; Rare:1077; Clinvar:44; Clinvar (benign):41 | ||||
| chr16:28847164-28847564 | Common:3; Rare:61 | ||||
| chr16:28861975-28862375 | Common:2; Rare:88 | ||||
| chr16:28863180-28864602 | Common:27; Rare:1055 | ||||
| chr16:28879777-28880180 | Common:22; Rare:479 | ||||
| chr16:28924778-28925716 | Common:6; Rare:718 | ||||
| chr16:28925640-28925922 | Rare:98 | ||||
| chr16:28936435-28936896 | Rare:767 | ||||
| chr16:28950401-28951215 | Common:11; Rare:772 | ||||
| chr16:28951242-28951642 | Common:3; Rare:265 |