| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66880348-66880617 | Common:2; Rare:67 | ||||
| chr16:66934360-66934499 | Common:1; Rare:51 | ||||
| chr16:67028933-67029105 | Rare:72 | ||||
| chr16:67159893-67160009 | Rare:20 | ||||
| chr16:67183923-67184111 | Common:1; Rare:58 | ||||
| chr16:67227008-67227189 | Rare:76 | ||||
| chr16:67247467-67247718 | Rare:78 | ||||
| chr16:67393413-67393654 | Common:1; Rare:59 | ||||
| chr16:67481045-67481384 | Common:1; Rare:122 | ||||
| chr16:67528681-67528883 | Rare:57 | ||||
| chr16:67545495-67545713 | Rare:71 | ||||
| chr16:67660222-67660373 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67666733-67666848 | Rare:23 | ||||
| chr16:67828495-67828770 | Rare:91 | ||||
| chr16:67935704-67935896 | Common:1; Rare:53 |