| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28846232-28846703 | Common:4; Rare:290; Clinvar:14; Clinvar (benign):12 | ||||
| chr16:28863297-28863559 | Common:1; Rare:101 | ||||
| chr16:28863633-28864018 | Common:5; Rare:142 | ||||
| chr16:28879873-28880061 | Common:6; Rare:103 | ||||
| chr16:28925167-28925412 | Rare:146 | ||||
| chr16:28925674-28925833 | Rare:56 | ||||
| chr16:28950602-28951040 | Common:2; Rare:237 | ||||
| chr16:28974638-28974834 | Common:1; Rare:150 | ||||
| chr16:29790433-29790807 | Common:3; Rare:252; Clinvar (benign):4 | ||||
| chr16:29798380-29798780 | Rare:172; Clinvar:3; Clinvar (pathogenic):4 | ||||
| chr16:29805482-29805768 | Common:4; Rare:255 | ||||
| chr16:29806158-29806896 | Common:7; Rare:353 | ||||
| chr16:29807660-29808270 | Common:4; Rare:327 | ||||
| chr16:29815927-29816550 | Common:7; Rare:346 | ||||
| chr16:29816901-29817301 | Rare:267 |