| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67246713-67246928 | Common:1; Rare:37 | ||||
| chr16:67247432-67247738 | Rare:97 | ||||
| chr16:67481028-67481380 | Common:1; Rare:122 | ||||
| chr16:67528664-67528883 | Rare:58 | ||||
| chr16:67562312-67562721 | Common:1; Rare:128 | ||||
| chr16:67660139-67660379 | Rare:119; Clinvar:3; Clinvar (benign):3 | ||||
| chr16:67666696-67666822 | Rare:27 | ||||
| chr16:67719264-67719478 | Common:1; Rare:60 | ||||
| chr16:67806537-67806939 | Rare:85 | ||||
| chr16:67806984-67807100 | Rare:33 | ||||
| chr16:67842020-67842333 | Common:2; Rare:94 | ||||
| chr16:67843412-67843684 | Rare:61 | ||||
| chr16:67843779-67844031 | Rare:41 | ||||
| chr16:67846352-67846770 | Common:2; Rare:118 | ||||
| chr16:67846773-67847268 | Common:2; Rare:130 |