| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57480144-57480307 | Common:1; Rare:29 | ||||
| chr12:57487758-57488147 | Common:1; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:57520377-57521059 | Common:4; Rare:186 | ||||
| chr12:57522143-57522450 | Common:1; Rare:65 | ||||
| chr12:57522527-57522956 | Common:4; Rare:160 | ||||
| chr12:57523191-57523294 | Rare:24 | ||||
| chr12:57546804-57546848 | Rare:10 | ||||
| chr12:57547068-57547242 | Common:2; Rare:45 | ||||
| chr12:57549884-57550089 | Rare:54 | ||||
| chr12:57590788-57590969 | Rare:32 | ||||
| chr12:57590998-57591350 | Common:6; Rare:150 | ||||
| chr12:57604805-57604887 | Rare:16 | ||||
| chr12:57605283-57605342 | Common:1; Rare:4 | ||||
| chr12:57611272-57611484 | Rare:42 | ||||
| chr12:57693859-57694235 | Common:1; Rare:108 |