| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56725130-56725605 | Common:3; Rare:130 | ||||
| chr12:57047988-57048314 | Rare:104; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:57087837-57088089 | Common:1; Rare:66 | ||||
| chr12:57111173-57111436 | Common:4; Rare:51 | ||||
| chr12:57111802-57111919 | Common:1; Rare:21 | ||||
| chr12:57128325-57128846 | Common:1; Rare:102 | ||||
| chr12:57128953-57128979 | Rare:6 | ||||
| chr12:57201555-57201893 | Common:2; Rare:72 | ||||
| chr12:57230022-57230190 | Rare:35 | ||||
| chr12:57488796-57489022 | Common:3; Rare:45; Clinvar (benign):1 | ||||
| chr12:57517101-57517361 | Rare:79 | ||||
| chr12:57520493-57520727 | Common:1; Rare:71 | ||||
| chr12:57522559-57522901 | Common:3; Rare:131 | ||||
| chr12:57524764-57525075 | Common:1; Rare:100 | ||||
| chr12:57526396-57526637 | Common:2; Rare:61 |