| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57772539-57772703 | Common:4; Rare:28 | ||||
| chr12:57818628-57818784 | Common:1; Rare:34 | ||||
| chr12:57846372-57846515 | Rare:46 | ||||
| chr12:57846677-57847221 | Common:4; Rare:190 | ||||
| chr12:57941360-57941688 | Common:3; Rare:96 | ||||
| chr12:58920483-58920667 | Common:2; Rare:66 | ||||
| chr12:59595789-59596196 | Common:7; Rare:87 | ||||
| chr12:62260026-62260482 | Common:1; Rare:168 | ||||
| chr12:62260815-62260847 | Rare:8 | ||||
| chr12:62260893-62260954 | Rare:9 | ||||
| chr12:63779749-63779921 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr12:63844716-63844819 | Rare:26 | ||||
| chr12:64222242-64222369 | Rare:41 | ||||
| chr12:64404258-64404661 | Common:5; Rare:145 | ||||
| chr12:64452004-64452171 | Common:1; Rare:60 |