| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53672409-53672591 | Common:1; Rare:39 | ||||
| chr12:55800854-55800933 | Rare:16 | ||||
| chr12:55889962-55890104 | Rare:22 | ||||
| chr12:56133865-56134125 | Common:1; Rare:51 | ||||
| chr12:56217167-56217350 | Common:1; Rare:30 | ||||
| chr12:56225370-56225694 | Rare:84 | ||||
| chr12:56423577-56423918 | Common:2; Rare:119 | ||||
| chr12:56634985-56635113 | Rare:21 | ||||
| chr12:56670347-56670477 | Common:1; Rare:33 | ||||
| chr12:57490309-57490615 | Rare:71; Clinvar:5; Clinvar (benign):3 | ||||
| chr12:57497931-57498445 | Common:3; Rare:159; Clinvar:3; Clinvar (benign):7 | ||||
| chr12:57546028-57546190 | Rare:40 | ||||
| chr12:57936018-57936273 | Common:4; Rare:69 | ||||
| chr12:62603487-62604028 | Common:2; Rare:156 | ||||
| chr12:62608309-62608527 | Common:3; Rare:49 |