| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105236035-105236265 | Common:2; Rare:101 | ||||
| chr12:106302745-106302871 | Common:4; Rare:42 | ||||
| chr12:106357483-106357823 | Common:4; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357988-106358111 | Common:3; Rare:48 | ||||
| chr12:106955453-106955907 | Common:3; Rare:169 | ||||
| chr12:106987040-106987286 | Common:4; Rare:69 | ||||
| chr12:108515070-108515319 | Common:1; Rare:76 | ||||
| chr12:108633872-108634003 | Rare:20 | ||||
| chr12:109052466-109052672 | Common:3; Rare:63 | ||||
| chr12:109154528-109154696 | Common:1; Rare:43 | ||||
| chr12:109477270-109477656 | Common:3; Rare:101 | ||||
| chr12:109573433-109573837 | Common:3; Rare:130; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880341-109880678 | Common:1; Rare:102 | ||||
| chr12:109999118-109999211 | Rare:13 | ||||
| chr12:110468673-110468915 | Rare:60 |