| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109309253-109309932 | Common:8; Rare:259 | ||||
| chr12:109458950-109459136 | Common:1; Rare:30 | ||||
| chr12:109477265-109477695 | Common:4; Rare:116 | ||||
| chr12:109573472-109573839 | Common:3; Rare:108; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109714120-109714334 | Common:2; Rare:58 | ||||
| chr12:109714368-109714768 | Common:5; Rare:145 | ||||
| chr12:109880380-109880790 | Common:2; Rare:108 | ||||
| chr12:109900159-109900332 | Rare:62 | ||||
| chr12:109996339-109996476 | Common:1; Rare:34 | ||||
| chr12:109999108-109999452 | Rare:76 | ||||
| chr12:110048473-110048790 | Common:1; Rare:80 | ||||
| chr12:110124128-110124474 | Common:2; Rare:109 | ||||
| chr12:110280360-110280730 | Rare:79 | ||||
| chr12:110280958-110281335 | Common:1; Rare:147; Clinvar (benign):1 | ||||
| chr12:110343185-110343585 | Common:1; Rare:137; Clinvar:2; Clinvar (benign):1 |