| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57742101-57742366 | Rare:59 | ||||
| chr12:57744801-57745165 | Common:1; Rare:86 | ||||
| chr12:57752192-57752665 | Rare:126; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:57754839-57755131 | Common:2; Rare:73 | ||||
| chr12:57771736-57771938 | Rare:42 | ||||
| chr12:57772043-57772305 | Rare:90 | ||||
| chr12:57772456-57772707 | Common:4; Rare:53 | ||||
| chr12:57782652-57782868 | Common:2; Rare:81; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:57845571-57845909 | Common:4; Rare:89 | ||||
| chr12:57846068-57846282 | Rare:62 | ||||
| chr12:57846920-57847239 | Common:3; Rare:119 | ||||
| chr12:57941106-57941622 | Common:5; Rare:135 | ||||
| chr12:57941630-57941812 | Rare:53 | ||||
| chr12:58919562-58919658 | Common:1; Rare:22 | ||||
| chr12:59595771-59596166 | Common:7; Rare:88 |