| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49060755-49060813 | Rare:21 | ||||
| chr12:49234560-49234711 | Common:1; Rare:45 | ||||
| chr12:49565142-49565272 | Rare:25 | ||||
| chr12:52032889-52033237 | Common:1; Rare:99 | ||||
| chr12:52057466-52057642 | Rare:54 | ||||
| chr12:53665004-53665294 | Common:1; Rare:43 | ||||
| chr12:53751903-53752153 | Common:2; Rare:47 | ||||
| chr12:55697215-55697477 | Common:2; Rare:70; Clinvar (benign):3 | ||||
| chr12:55709733-55710165 | Common:5; Rare:74 | ||||
| chr12:56190243-56190346 | Common:1; Rare:49 | ||||
| chr12:56634993-56635223 | Common:1; Rare:41 | ||||
| chr12:57239149-57239416 | Common:1; Rare:62 | ||||
| chr12:57605670-57605804 | Common:2; Rare:18 | ||||
| chr12:57618015-57618366 | Common:4; Rare:79 | ||||
| chr12:57803564-57803785 | Common:1; Rare:66 |