| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8949975-8950095 | Common:1; Rare:33 | ||||
| chr12:10613540-10613646 | Common:1; Rare:44 | ||||
| chr12:11170950-11171237 | Common:2; Rare:79 | ||||
| chr12:11171549-11171701 | Common:2; Rare:50 | ||||
| chr12:12357015-12357182 | Common:4; Rare:90 | ||||
| chr12:12611539-12612019 | Common:3; Rare:141 | ||||
| chr12:12684464-12684783 | Common:1; Rare:42 | ||||
| chr12:12717072-12717480 | Rare:137; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725649-12725929 | Common:2; Rare:60 | ||||
| chr12:13980573-13980949 | Common:1; Rare:85 | ||||
| chr12:13981518-13981662 | Common:2; Rare:24 | ||||
| chr12:14365374-14365714 | Common:1; Rare:104 | ||||
| chr12:14803461-14803715 | Common:1; Rare:68 | ||||
| chr12:15322409-15322633 | Rare:53 | ||||
| chr12:15780725-15781028 | Rare:55 |