| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67183941-67184040 | Common:1; Rare:29 | ||||
| chr16:67199098-67199170 | Common:1; Rare:29 | ||||
| chr16:67226994-67227196 | Rare:86 | ||||
| chr16:67237533-67237804 | Rare:91 | ||||
| chr16:67247469-67247742 | Rare:81 | ||||
| chr16:67279255-67279555 | Common:1; Rare:83 | ||||
| chr16:67393380-67393670 | Common:1; Rare:66 | ||||
| chr16:67396300-67396599 | Common:1; Rare:77 | ||||
| chr16:67481037-67481384 | Common:1; Rare:123 | ||||
| chr16:67528706-67528861 | Rare:43 | ||||
| chr16:67537440-67537501 | Common:1; Rare:11 | ||||
| chr16:67545789-67545975 | Common:1; Rare:55 | ||||
| chr16:67660207-67660391 | Rare:110; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67666728-67666839 | Rare:21 | ||||
| chr16:67719273-67719546 | Common:1; Rare:77 |