| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064435-104064555 | Rare:29 | ||||
| chr12:104138170-104138403 | Common:1; Rare:62 | ||||
| chr12:104286937-104287077 | Common:2; Rare:38 | ||||
| chr12:104287204-104287313 | Rare:25 | ||||
| chr12:104986210-104986347 | Common:2; Rare:41 | ||||
| chr12:105107609-105107795 | Common:1; Rare:85 | ||||
| chr12:105236041-105236300 | Common:2; Rare:112 | ||||
| chr12:106357676-106357728 | Common:1; Rare:12; Clinvar:1 | ||||
| chr12:106357730-106357823 | Common:2; Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:106684668-106684803 | Common:3; Rare:24 | ||||
| chr12:106955635-106955907 | Rare:97 | ||||
| chr12:107320246-107320469 | Rare:40 | ||||
| chr12:107685629-107685895 | Common:2; Rare:87 | ||||
| chr12:108339297-108339406 | Rare:27 | ||||
| chr12:108515054-108515313 | Common:1; Rare:78 |