| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105233806-105233936 | Rare:26 | ||||
| chr12:105236004-105236279 | Common:3; Rare:111 | ||||
| chr12:106357676-106357812 | Common:3; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:108515030-108515313 | Common:1; Rare:85 | ||||
| chr12:108538159-108538478 | Common:4; Rare:65 | ||||
| chr12:108562399-108562686 | Common:9; Rare:122; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633788-108634043 | Rare:52 | ||||
| chr12:109052504-109052684 | Common:2; Rare:59 | ||||
| chr12:109097847-109098221 | Common:5; Rare:118 | ||||
| chr12:109154557-109154691 | Common:1; Rare:35 | ||||
| chr12:109477287-109477679 | Common:3; Rare:103 | ||||
| chr12:109573430-109573869 | Common:3; Rare:143; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:109880327-109880676 | Common:1; Rare:109 | ||||
| chr12:109908326-109908526 | Common:1; Rare:36 | ||||
| chr12:109914196-109914373 | Rare:34 |