| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57088809-57089158 | Common:2; Rare:128 | ||||
| chr12:57110372-57110453 | Common:1; Rare:15 | ||||
| chr12:57110570-57110746 | Rare:33 | ||||
| chr12:57111762-57111917 | Common:1; Rare:32 | ||||
| chr12:57229556-57229815 | Common:3; Rare:104 | ||||
| chr12:57230007-57230142 | Rare:27 | ||||
| chr12:57230155-57230199 | Rare:8 | ||||
| chr12:57430419-57430579 | Common:1; Rare:43 | ||||
| chr12:57430684-57431253 | Common:5; Rare:164 | ||||
| chr12:57476228-57476517 | Common:3; Rare:92; Clinvar:1 | ||||
| chr12:57477181-57477431 | Rare:58 | ||||
| chr12:57477760-57478263 | Common:2; Rare:117 | ||||
| chr12:57479578-57480042 | Common:1; Rare:84 | ||||
| chr12:57480175-57480262 | Common:1; Rare:13 | ||||
| chr12:57487786-57488142 | Common:1; Rare:83; Clinvar:3; Clinvar (benign):1 |