| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23557342-23557552 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641287-23641530 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:24729632-24729754 | Common:6; Rare:69 | ||||
| chr16:25111474-25111755 | Common:2; Rare:65 | ||||
| chr16:27268711-27268866 | Common:1; Rare:57 | ||||
| chr16:27549891-27550160 | Common:2; Rare:94 | ||||
| chr16:28538659-28538705 | Rare:13 | ||||
| chr16:28823958-28824082 | Rare:30 | ||||
| chr16:28846271-28846698 | Common:2; Rare:141; Clinvar:5; Clinvar (benign):5 | ||||
| chr16:28925165-28925405 | Rare:78 | ||||
| chr16:29808081-29808211 | Rare:61 | ||||
| chr16:29926180-29926340 | Common:3; Rare:60 | ||||
| chr16:29995606-29995714 | Rare:49 | ||||
| chr16:29996069-29996262 | Common:2; Rare:66 | ||||
| chr16:30069533-30070001 | Common:1; Rare:173; Clinvar:6; Clinvar (benign):6 |