| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57128313-57128728 | Common:1; Rare:80 | ||||
| chr12:57201553-57201833 | Common:2; Rare:64 | ||||
| chr12:57229387-57229746 | Common:3; Rare:114 | ||||
| chr12:57430729-57431090 | Common:1; Rare:94 | ||||
| chr12:57475819-57476085 | Rare:72 | ||||
| chr12:57489959-57490294 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:57520501-57520734 | Common:1; Rare:70 | ||||
| chr12:57521751-57521826 | Rare:14 | ||||
| chr12:57522497-57522901 | Common:3; Rare:149 | ||||
| chr12:57533991-57534310 | Rare:86 | ||||
| chr12:57547089-57547299 | Common:1; Rare:48 | ||||
| chr12:57591096-57591454 | Common:6; Rare:151 | ||||
| chr12:57604658-57604857 | Rare:38 | ||||
| chr12:57610242-57610314 | Common:1; Rare:34 | ||||
| chr12:57611234-57611404 | Rare:34 |