| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110280950-110281820 | Common:4; Rare:287; Clinvar:3; Clinvar (benign):7 | ||||
| chr12:110281824-110282035 | Common:1; Rare:57; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:110282158-110282413 | Common:1; Rare:59 | ||||
| chr12:110403196-110403348 | Rare:42 | ||||
| chr12:110403399-110403534 | Common:1; Rare:30 | ||||
| chr12:110403578-110403745 | Common:2; Rare:88 | ||||
| chr12:110404035-110404224 | Common:4; Rare:43 | ||||
| chr12:110449792-110449901 | Rare:16 | ||||
| chr12:110450048-110450133 | Rare:21 | ||||
| chr12:110450220-110450515 | Common:2; Rare:98 | ||||
| chr12:110468113-110468598 | Common:3; Rare:162 | ||||
| chr12:110468648-110468948 | Rare:88 | ||||
| chr12:110469101-110469383 | Common:1; Rare:53 | ||||
| chr12:110501344-110501785 | Common:1; Rare:139 | ||||
| chr12:110501838-110502381 | Common:1; Rare:214 |