| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:42326032-42326182 | Common:1; Rare:51 | ||||
| chr12:43758753-43758991 | Common:2; Rare:66; Clinvar:2 | ||||
| chr12:45216007-45216140 | Rare:43 | ||||
| chr12:46372759-46372923 | Rare:72 | ||||
| chr12:47079521-47079629 | Common:1; Rare:22 | ||||
| chr12:47705972-47706088 | Rare:55 | ||||
| chr12:47758878-47758986 | Rare:27 | ||||
| chr12:47904992-47905117 | Common:1; Rare:35; Clinvar:1 | ||||
| chr12:48105846-48105938 | Rare:21 | ||||
| chr12:49367245-49367524 | Common:1; Rare:77 | ||||
| chr12:49568104-49568194 | Common:2; Rare:30 | ||||
| chr12:50763931-50764113 | Common:1; Rare:51 | ||||
| chr12:51026314-51026510 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:52451666-52451882 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr12:52493219-52493422 | Rare:38 |