| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68023204-68023336 | Common:1; Rare:38 | ||||
| chr16:68085152-68085406 | Common:2; Rare:50 | ||||
| chr16:68310927-68311084 | Common:1; Rare:78 | ||||
| chr16:68539167-68539330 | Common:1; Rare:82 | ||||
| chr16:69132521-69132673 | Rare:57 | ||||
| chr16:69339505-69339849 | Common:2; Rare:157; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:69726448-69726534 | Rare:28 | ||||
| chr16:69726556-69726818 | Common:3; Rare:60 | ||||
| chr16:69762274-69762381 | Common:1; Rare:27 | ||||
| chr16:70289395-70289649 | Rare:89; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:70299068-70299222 | Common:1; Rare:29 | ||||
| chr16:70346751-70346951 | Common:1; Rare:99 | ||||
| chr16:70523517-70523847 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71809057-71809338 | Common:3; Rare:92 | ||||
| chr16:71845830-71846020 | Common:2; Rare:62 |