| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66934357-66934537 | Common:1; Rare:67 | ||||
| chr16:67226859-67227187 | Common:1; Rare:121 | ||||
| chr16:67481079-67481384 | Common:1; Rare:114 | ||||
| chr16:68023212-68023296 | Common:1; Rare:19 | ||||
| chr16:68310932-68311084 | Common:1; Rare:77 | ||||
| chr16:69132553-69132672 | Rare:46 | ||||
| chr16:69339548-69339824 | Common:1; Rare:113; Clinvar (benign):1 | ||||
| chr16:69726446-69726868 | Common:3; Rare:109 | ||||
| chr16:70346779-70346908 | Common:1; Rare:58 | ||||
| chr16:70523532-70523846 | Common:3; Rare:101; Clinvar (pathogenic):1 | ||||
| chr16:72008511-72008775 | Common:5; Rare:96; Clinvar (benign):1 | ||||
| chr16:72093605-72093934 | Rare:75 | ||||
| chr16:74666853-74667116 | Common:1; Rare:86 | ||||
| chr16:75647629-75647863 | Common:4; Rare:116; Clinvar:4 | ||||
| chr16:84116787-84117092 | Common:3; Rare:125 |