| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57751824-57751986 | Rare:25 | ||||
| chr12:57772087-57772244 | Rare:55 | ||||
| chr12:57772516-57772665 | Common:2; Rare:22 | ||||
| chr12:57846392-57846487 | Rare:30 | ||||
| chr12:57846920-57847221 | Common:2; Rare:110 | ||||
| chr12:57941393-57941704 | Common:3; Rare:92 | ||||
| chr12:57941717-57941742 | Rare:10 | ||||
| chr12:62260042-62260441 | Common:1; Rare:150 | ||||
| chr12:63780065-63780171 | Rare:50; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:64222242-64222346 | Rare:35 | ||||
| chr12:64759373-64759496 | Common:1; Rare:41; Clinvar:3 | ||||
| chr12:65825004-65825136 | Rare:34 | ||||
| chr12:66130710-66130861 | Rare:53 | ||||
| chr12:66189146-66189295 | Rare:37 | ||||
| chr12:68610695-68611005 | Common:1; Rare:138 |