| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12562825-12563023 | Common:2; Rare:110 | ||||
| chr12:12611627-12611971 | Common:4; Rare:176 | ||||
| chr12:12716956-12717560 | Common:4; Rare:356; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:12725234-12726003 | Common:11; Rare:245 | ||||
| chr12:12813050-12813380 | Common:4; Rare:158 | ||||
| chr12:12890530-12890820 | Common:2; Rare:100 | ||||
| chr12:12891236-12891748 | Common:3; Rare:171 | ||||
| chr12:13000212-13000513 | Common:4; Rare:178 | ||||
| chr12:13044289-13044424 | Rare:36 | ||||
| chr12:13196554-13196866 | Common:1; Rare:51 | ||||
| chr12:14365466-14365818 | Common:2; Rare:174 | ||||
| chr12:14365787-14366210 | Rare:197 | ||||
| chr12:14770955-14771271 | Common:2; Rare:149 | ||||
| chr12:14774184-14774516 | Common:6; Rare:163 | ||||
| chr12:14802920-14803380 | Common:10; Rare:176 |