| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121626233-121626709 | Common:2; Rare:177 | ||||
| chr12:121626735-121626935 | Common:5; Rare:116; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:121627206-121627624 | Common:2; Rare:78 | ||||
| chr12:121672586-121672808 | Common:5; Rare:71 | ||||
| chr12:121712586-121712859 | Common:5; Rare:107 | ||||
| chr12:121792854-121793146 | Common:2; Rare:68 | ||||
| chr12:121793613-121793753 | Common:1; Rare:52 | ||||
| chr12:121793962-121794126 | Common:2; Rare:41 | ||||
| chr12:121794260-121794533 | Common:1; Rare:75 | ||||
| chr12:121799994-121800390 | Common:3; Rare:114 | ||||
| chr12:121800510-121800823 | Common:1; Rare:87 | ||||
| chr12:121800892-121801298 | Common:5; Rare:118 | ||||
| chr12:121802832-121803167 | Common:1; Rare:81 | ||||
| chr12:121803196-121803621 | Common:1; Rare:117 | ||||
| chr12:121803869-121804396 | Rare:178 |