| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67968568-67968856 | Common:2; Rare:98 | ||||
| chr16:68023209-68023296 | Common:1; Rare:22 | ||||
| chr16:68245192-68245402 | Common:1; Rare:66 | ||||
| chr16:68310868-68311062 | Common:1; Rare:102 | ||||
| chr16:68530049-68530144 | Common:4; Rare:45 | ||||
| chr16:68644675-68644946 | Common:2; Rare:63; Clinvar:5; Clinvar (benign):2 | ||||
| chr16:69132541-69132671 | Rare:54 | ||||
| chr16:69339562-69339821 | Common:1; Rare:103; Clinvar (benign):1 | ||||
| chr16:69726537-69726868 | Common:3; Rare:78 | ||||
| chr16:69762288-69762381 | Rare:22 | ||||
| chr16:70114214-70114376 | Common:1; Rare:62 | ||||
| chr16:70289440-70289678 | Rare:84; Clinvar:1 | ||||
| chr16:70346809-70346947 | Common:1; Rare:68 | ||||
| chr16:70523532-70523899 | Common:3; Rare:116; Clinvar (pathogenic):1 | ||||
| chr16:71564938-71565011 | Rare:26 |