| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29996072-29996296 | Common:2; Rare:79 | ||||
| chr16:30064333-30064493 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr16:30065523-30065889 | Rare:124 | ||||
| chr16:30075894-30076034 | Rare:47 | ||||
| chr16:30123073-30123375 | Common:6; Rare:88 | ||||
| chr16:30183477-30183623 | Common:1; Rare:37 | ||||
| chr16:30355211-30355431 | Common:1; Rare:75 | ||||
| chr16:30375858-30376219 | Rare:85 | ||||
| chr16:30534867-30535105 | Common:3; Rare:80 | ||||
| chr16:30585537-30585612 | Rare:22 | ||||
| chr16:30698057-30698235 | Rare:97 | ||||
| chr16:30762082-30762343 | Common:3; Rare:88 | ||||
| chr16:30787118-30787468 | Common:1; Rare:74 | ||||
| chr16:30893927-30894268 | Common:5; Rare:93 | ||||
| chr16:30896523-30896630 | Rare:26 |