| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68023209-68023307 | Common:1; Rare:27 | ||||
| chr16:68245151-68245417 | Common:1; Rare:79 | ||||
| chr16:68310918-68311081 | Common:1; Rare:81 | ||||
| chr16:69132532-69132680 | Rare:61 | ||||
| chr16:69187012-69187169 | Rare:59 | ||||
| chr16:69339548-69339850 | Common:1; Rare:131; Clinvar (benign):1 | ||||
| chr16:69424489-69424686 | Rare:57 | ||||
| chr16:69566262-69566330 | Rare:19 | ||||
| chr16:69726435-69726819 | Common:4; Rare:103 | ||||
| chr16:69762266-69762381 | Common:1; Rare:28 | ||||
| chr16:70114118-70114392 | Common:3; Rare:99 | ||||
| chr16:70346759-70346977 | Common:2; Rare:107 | ||||
| chr16:70454517-70454619 | Common:1; Rare:29 | ||||
| chr16:70523530-70523861 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
| chr16:71808774-71808875 | Common:1; Rare:58 |