| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109052442-109052654 | Common:3; Rare:61 | ||||
| chr12:109093373-109093642 | Common:2; Rare:101 | ||||
| chr12:109097367-109097716 | Rare:117; Clinvar:3 | ||||
| chr12:109097886-109098244 | Common:5; Rare:114 | ||||
| chr12:109154523-109154771 | Common:2; Rare:62 | ||||
| chr12:109154998-109155294 | Common:2; Rare:56 | ||||
| chr12:109309685-109309966 | Rare:90 | ||||
| chr12:109476997-109477049 | Rare:9 | ||||
| chr12:109477222-109477709 | Common:4; Rare:135 | ||||
| chr12:109477868-109477918 | Rare:15 | ||||
| chr12:109573106-109573398 | Common:3; Rare:75 | ||||
| chr12:109573438-109573917 | Common:3; Rare:156; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr12:109713954-109713985 | Rare:8 | ||||
| chr12:109714194-109714432 | Common:4; Rare:60 | ||||
| chr12:109880423-109880808 | Common:2; Rare:94 |