| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107685695-107685939 | Rare:79 | ||||
| chr12:107760963-107761279 | Common:4; Rare:123 | ||||
| chr12:108339272-108339381 | Rare:28 | ||||
| chr12:108515024-108515319 | Common:1; Rare:90 | ||||
| chr12:108531940-108532089 | Common:1; Rare:28 | ||||
| chr12:108538072-108538324 | Common:2; Rare:57 | ||||
| chr12:108561098-108561448 | Common:3; Rare:95 | ||||
| chr12:108562473-108562731 | Common:9; Rare:116; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108731489-108731686 | Common:2; Rare:72 | ||||
| chr12:109052460-109052667 | Common:3; Rare:64 | ||||
| chr12:109052825-109052902 | Rare:10 | ||||
| chr12:109093393-109093530 | Rare:51 | ||||
| chr12:109093610-109093637 | Rare:10 | ||||
| chr12:109097509-109097677 | Rare:65; Clinvar:2 | ||||
| chr12:109097920-109098274 | Common:5; Rare:103 |