| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57489869-57490269 | Common:4; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr12:57514755-57515155 | Common:3; Rare:117; Clinvar:5; Clinvar (benign):6 | ||||
| chr12:57515298-57515698 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr12:57516947-57517347 | Rare:136 | ||||
| chr12:57517397-57517797 | Common:3; Rare:123 | ||||
| chr12:57519618-57520240 | Common:3; Rare:196 | ||||
| chr12:57520200-57521363 | Common:22; Rare:983 | ||||
| chr12:57521739-57521880 | Common:2; Rare:56 | ||||
| chr12:57521980-57522482 | Common:4; Rare:285 | ||||
| chr12:57522451-57523283 | Common:18; Rare:939 | ||||
| chr12:57523483-57523942 | Common:11; Rare:174 | ||||
| chr12:57524716-57525160 | Common:3; Rare:311 | ||||
| chr12:57528130-57528530 | Common:2; Rare:126 | ||||
| chr12:57547099-57547504 | Common:7; Rare:418 | ||||
| chr12:57548979-57549546 | Common:4; Rare:136 |