| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28844720-28844983 | Rare:89; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:28846256-28846715 | Common:2; Rare:151; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:28863492-28863991 | Common:3; Rare:124 | ||||
| chr16:28879898-28880036 | Common:3; Rare:41 | ||||
| chr16:28974665-28974792 | Rare:57 | ||||
| chr16:29790566-29790788 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr16:29807746-29808165 | Common:2; Rare:218 | ||||
| chr16:29816018-29816225 | Common:1; Rare:57 | ||||
| chr16:29863808-29863878 | Rare:22 | ||||
| chr16:29926029-29926316 | Common:2; Rare:105 | ||||
| chr16:29961950-29962171 | Common:1; Rare:72 | ||||
| chr16:29973613-29973899 | Common:4; Rare:94 | ||||
| chr16:29995610-29995713 | Rare:47 | ||||
| chr16:29996072-29996313 | Common:2; Rare:88 | ||||
| chr16:30065575-30065912 | Rare:111 |