| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28554172-28554347 | Common:5; Rare:96 | ||||
| chr16:28597012-28597215 | Common:4; Rare:122 | ||||
| chr16:28597382-28597782 | Common:6; Rare:85 | ||||
| chr16:28609945-28610461 | Common:14; Rare:173 | ||||
| chr16:28822608-28822759 | Rare:62 | ||||
| chr16:28822905-28823300 | Common:8; Rare:257 | ||||
| chr16:28823476-28824566 | Common:11; Rare:540 | ||||
| chr16:28845346-28845663 | Common:4; Rare:152; Clinvar (pathogenic):2 | ||||
| chr16:28846234-28846715 | Common:4; Rare:313; Clinvar:12; Clinvar (benign):12 | ||||
| chr16:28863170-28863590 | Common:6; Rare:152 | ||||
| chr16:28863724-28864093 | Common:6; Rare:178 | ||||
| chr16:28925133-28925412 | Rare:158 | ||||
| chr16:28936475-28936865 | Rare:181 | ||||
| chr16:28950560-28951017 | Common:2; Rare:146 | ||||
| chr16:28974667-28974889 | Rare:187 |