| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28846253-28846715 | Common:2; Rare:153; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:28863713-28864016 | Common:3; Rare:80 | ||||
| chr16:28925167-28925375 | Rare:67 | ||||
| chr16:28974056-28974141 | Common:1; Rare:25 | ||||
| chr16:28974669-28974792 | Rare:56 | ||||
| chr16:29454239-29454590 | |||||
| chr16:29790422-29790794 | Common:2; Rare:135; Clinvar (benign):2 | ||||
| chr16:29805466-29805641 | Common:1; Rare:83 | ||||
| chr16:29807490-29808157 | Common:3; Rare:310 | ||||
| chr16:29811091-29811380 | Rare:122 | ||||
| chr16:29815936-29816190 | Common:2; Rare:75 | ||||
| chr16:29816285-29816476 | Common:1; Rare:56 | ||||
| chr16:29898979-29899301 | Common:2; Rare:68 | ||||
| chr16:29900096-29900713 | Common:4; Rare:148 | ||||
| chr16:29900763-29900872 | Rare:16 |