| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4538436-4538942 | Common:3; Rare:115 | ||||
| chr12:6451819-6452135 | Common:4; Rare:61 | ||||
| chr12:6493094-6493386 | Common:7; Rare:88 | ||||
| chr12:6493834-6494140 | Common:2; Rare:89 | ||||
| chr12:6534393-6534615 | Common:5; Rare:90 | ||||
| chr12:6568255-6568371 | Rare:44 | ||||
| chr12:6591483-6591696 | Rare:54 | ||||
| chr12:6723852-6724333 | Common:2; Rare:103 | ||||
| chr12:6766660-6766741 | Rare:23 | ||||
| chr12:6851227-6851557 | Common:1; Rare:78 | ||||
| chr12:6867651-6867671 | Rare:6 | ||||
| chr12:6873282-6873479 | Common:2; Rare:56 | ||||
| chr12:6943528-6943833 | Common:4; Rare:136 | ||||
| chr12:6970415-6971080 | Common:9; Rare:210; Clinvar (benign):2 | ||||
| chr12:7108497-7108681 | Common:1; Rare:49 |