| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67935587-67935982 | Common:2; Rare:134 | ||||
| chr16:67936824-67937088 | Common:1; Rare:42 | ||||
| chr16:68023207-68023325 | Common:1; Rare:32 | ||||
| chr16:68234525-68234806 | Rare:41 | ||||
| chr16:68235316-68235484 | Rare:35 | ||||
| chr16:68245161-68245417 | Common:1; Rare:76 | ||||
| chr16:68264437-68264663 | Rare:67 | ||||
| chr16:68310865-68311062 | Common:1; Rare:105 | ||||
| chr16:68363854-68363957 | Common:2; Rare:30 | ||||
| chr16:68539169-68539323 | Common:1; Rare:77 | ||||
| chr16:68737159-68737463 | Common:2; Rare:108; Clinvar:11; Clinvar (benign):23 | ||||
| chr16:68808466-68808848 | Common:2; Rare:84; Clinvar:25; Clinvar (benign):19; Clinvar (pathogenic):1 | ||||
| chr16:68823131-68823485 | Common:3; Rare:72; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:69132547-69132663 | Rare:47 | ||||
| chr16:69187011-69187169 | Rare:60 |