| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56111226-56111524 | Rare:74 | ||||
| chr12:56132207-56132595 | Rare:116 | ||||
| chr12:56133612-56133806 | Rare:45 | ||||
| chr12:56225279-56225495 | Rare:39 | ||||
| chr12:56355425-56355791 | Common:1; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:56509103-56509350 | Rare:51 | ||||
| chr12:56634993-56635057 | Rare:15 | ||||
| chr12:57089830-57090120 | Common:1; Rare:76 | ||||
| chr12:57205353-57205678 | Rare:97 | ||||
| chr12:57210031-57210472 | Rare:110 | ||||
| chr12:57211217-57211468 | Common:1; Rare:70 | ||||
| chr12:57213288-57213434 | Common:1; Rare:14 | ||||
| chr12:57371516-57371524 | Rare:1 | ||||
| chr12:57462787-57462902 | Common:1; Rare:27 | ||||
| chr12:57837063-57837119 | Rare:5 |