| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30065560-30065923 | Rare:125 | ||||
| chr16:30069488-30070038 | Common:1; Rare:203; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30075889-30076045 | Rare:51 | ||||
| chr16:30123079-30123375 | Common:6; Rare:86 | ||||
| chr16:30355211-30355350 | Common:1; Rare:55 | ||||
| chr16:30445867-30446050 | Common:1; Rare:44 | ||||
| chr16:30526762-30526830 | Common:4; Rare:25 | ||||
| chr16:30534824-30535091 | Common:3; Rare:84 | ||||
| chr16:30571558-30571711 | Rare:46 | ||||
| chr16:30572143-30572244 | Rare:29 | ||||
| chr16:30585531-30585912 | Common:1; Rare:88 | ||||
| chr16:30698459-30698727 | Common:1; Rare:98 | ||||
| chr16:30748148-30748447 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762058-30762343 | Common:3; Rare:93 | ||||
| chr16:30787113-30787296 | Rare:33 |