| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67481070-67481380 | Common:1; Rare:114 | ||||
| chr16:67528654-67528886 | Rare:58 | ||||
| chr16:67666707-67666853 | Rare:31 | ||||
| chr16:67806542-67806856 | Rare:62 | ||||
| chr16:67807011-67807089 | Rare:18 | ||||
| chr16:67843305-67843605 | Rare:52 | ||||
| chr16:68023209-68023302 | Common:1; Rare:25 | ||||
| chr16:68310927-68311084 | Common:1; Rare:78 | ||||
| chr16:69132540-69132680 | Rare:60 | ||||
| chr16:69339541-69339824 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:69726448-69726856 | Common:3; Rare:104 | ||||
| chr16:70346759-70346933 | Common:1; Rare:82 | ||||
| chr16:70454543-70454598 | Rare:13 | ||||
| chr16:70523489-70523857 | Common:3; Rare:133; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:72093550-72093937 | Rare:99 |