| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28863927-28864001 | Rare:16 | ||||
| chr16:28925144-28925271 | Rare:36 | ||||
| chr16:28925712-28925952 | Common:1; Rare:40 | ||||
| chr16:28974548-28974796 | Common:2; Rare:82 | ||||
| chr16:29454301-29454646 | |||||
| chr16:29807826-29808144 | Common:2; Rare:180 | ||||
| chr16:29862469-29862712 | Common:1; Rare:54 | ||||
| chr16:29863121-29863530 | Rare:104 | ||||
| chr16:29961994-29962141 | Common:1; Rare:43 | ||||
| chr16:29995601-29995744 | Rare:63 | ||||
| chr16:29996070-29996313 | Common:2; Rare:89 | ||||
| chr16:30065575-30065923 | Rare:118 | ||||
| chr16:30069490-30070046 | Common:1; Rare:207; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30075905-30076078 | Common:1; Rare:62 | ||||
| chr16:30117738-30117831 | Rare:23 |