| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30021170-30021601 | Rare:146 | ||||
| chr16:30052883-30053283 | Common:7; Rare:616; Clinvar (benign):6 | ||||
| chr16:30053651-30053792 | Rare:24 | ||||
| chr16:30063675-30064508 | Common:4; Rare:509; Clinvar (benign):4 | ||||
| chr16:30064434-30065300 | Common:1; Rare:435; Clinvar (benign):1 | ||||
| chr16:30065227-30065358 | Rare:27 | ||||
| chr16:30065288-30065956 | Rare:975 | ||||
| chr16:30065908-30066767 | Common:4; Rare:594 | ||||
| chr16:30066861-30067836 | Common:6; Rare:669; Clinvar:21; Clinvar (benign):9 | ||||
| chr16:30069431-30069906 | Common:3; Rare:254; Clinvar:4; Clinvar (benign):11 | ||||
| chr16:30069980-30070422 | Common:3; Rare:209; Clinvar:5; Clinvar (benign):7 | ||||
| chr16:30075758-30076158 | Common:7; Rare:555 | ||||
| chr16:30091743-30092662 | Common:10; Rare:665; Clinvar (pathogenic):3 | ||||
| chr16:30096112-30096540 | Common:4; Rare:427 | ||||
| chr16:30108477-30108877 | Rare:107 |