| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57520432-57520720 | Common:2; Rare:84 | ||||
| chr12:57522472-57522701 | Rare:65 | ||||
| chr12:57524390-57525134 | Common:2; Rare:344 | ||||
| chr12:57547151-57547378 | Common:1; Rare:42 | ||||
| chr12:57549947-57550075 | Rare:35 | ||||
| chr12:57591064-57591289 | Common:5; Rare:105 | ||||
| chr12:57611130-57611454 | Rare:67 | ||||
| chr12:57612327-57612761 | Common:1; Rare:126 | ||||
| chr12:57631665-57632961 | Common:11; Rare:458; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:57633153-57633321 | Common:1; Rare:55 | ||||
| chr12:57744767-57745072 | Rare:62 | ||||
| chr12:57752475-57752736 | Common:1; Rare:67 | ||||
| chr12:57771728-57771909 | Rare:37 | ||||
| chr12:57772022-57772251 | Rare:91 | ||||
| chr12:57772487-57772835 | Common:5; Rare:87 |