| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118103143-118103331 | Common:1; Rare:39 | ||||
| chr12:118103415-118103649 | Common:2; Rare:56 | ||||
| chr12:118103668-118104162 | Common:2; Rare:117 | ||||
| chr12:118135914-118136390 | Common:3; Rare:135 | ||||
| chr12:118372643-118372652 | Rare:1 | ||||
| chr12:118372795-118373265 | Common:3; Rare:138 | ||||
| chr12:118376210-118376577 | Common:1; Rare:109 | ||||
| chr12:118376819-118376881 | Rare:23 | ||||
| chr12:119178695-119179001 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:119667847-119668304 | Common:3; Rare:123 | ||||
| chr12:119668434-119668695 | Common:2; Rare:51 | ||||
| chr12:119877265-119877603 | Common:2; Rare:70 | ||||
| chr12:120090907-120091017 | Rare:18 | ||||
| chr12:120116305-120116441 | Rare:32 | ||||
| chr12:120116585-120117068 | Common:9; Rare:146 |