| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53061251-53061429 | Common:3; Rare:53 | ||||
| chr12:53063092-53063414 | Rare:86 | ||||
| chr12:53079335-53079415 | Rare:38 | ||||
| chr12:53097330-53097795 | Common:2; Rare:106 | ||||
| chr12:53180459-53180603 | Common:1; Rare:57 | ||||
| chr12:53180610-53180802 | Common:1; Rare:72 | ||||
| chr12:53180896-53181083 | Common:3; Rare:56 | ||||
| chr12:53181317-53181563 | Rare:68 | ||||
| chr12:53232174-53232432 | Common:2; Rare:55 | ||||
| chr12:53252049-53252208 | Common:3; Rare:61 | ||||
| chr12:53321232-53321423 | Common:1; Rare:69; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53321548-53321905 | Common:1; Rare:61; Clinvar:1 | ||||
| chr12:53380591-53380861 | Common:1; Rare:88 | ||||
| chr12:53499428-53499713 | Rare:64 | ||||
| chr12:53501213-53501357 | Rare:35 |