| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56468454-56468584 | Rare:59 | ||||
| chr12:56521781-56522089 | Common:3; Rare:78 | ||||
| chr12:56636303-56636436 | Rare:27 | ||||
| chr12:56644921-56645286 | Rare:81 | ||||
| chr12:56645835-56646297 | Common:1; Rare:136 | ||||
| chr12:56687993-56688062 | Rare:32 | ||||
| chr12:56688113-56688508 | Common:5; Rare:141 | ||||
| chr12:56725494-56725603 | Rare:23 | ||||
| chr12:56752313-56752457 | Rare:46 | ||||
| chr12:57087837-57088101 | Common:1; Rare:71 | ||||
| chr12:57111160-57111464 | Common:4; Rare:57 | ||||
| chr12:57111756-57111903 | Common:1; Rare:31 | ||||
| chr12:57128345-57129031 | Common:1; Rare:139 | ||||
| chr12:57201496-57201862 | Common:2; Rare:87 | ||||
| chr12:57489956-57490296 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):2 |