| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121352326-121352657 | Common:6; Rare:244 | ||||
| chr12:121399818-121400193 | Common:10; Rare:260 | ||||
| chr12:121536960-121537500 | Common:6; Rare:206 | ||||
| chr12:121537552-121537702 | Common:2; Rare:52 | ||||
| chr12:121538103-121538248 | Common:1; Rare:39 | ||||
| chr12:121580241-121580519 | Rare:81 | ||||
| chr12:121626276-121626828 | Common:5; Rare:360; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:121672462-121672862 | Common:17; Rare:260 | ||||
| chr12:121712641-121712923 | Common:6; Rare:178 | ||||
| chr12:121793928-121794118 | Common:3; Rare:84 | ||||
| chr12:121794170-121794500 | Common:2; Rare:161 | ||||
| chr12:121799911-121800330 | Common:4; Rare:192 | ||||
| chr12:121800380-121800818 | Common:5; Rare:216 | ||||
| chr12:121802904-121803393 | Common:2; Rare:234 | ||||
| chr12:121803896-121804120 | Rare:128 |