| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:42326065-42326218 | Common:1; Rare:49 | ||||
| chr12:43758743-43759021 | Common:2; Rare:78; Clinvar:2 | ||||
| chr12:43806241-43806418 | Common:2; Rare:60 | ||||
| chr12:45215987-45216382 | Common:1; Rare:131 | ||||
| chr12:45729413-45729747 | Common:1; Rare:90 | ||||
| chr12:45990416-45990961 | Common:3; Rare:175 | ||||
| chr12:46371374-46371549 | Common:2; Rare:79 | ||||
| chr12:46372725-46372933 | Rare:91 | ||||
| chr12:46832427-46832487 | Rare:9 | ||||
| chr12:47079521-47079651 | Common:1; Rare:25 | ||||
| chr12:47705960-47706124 | Rare:70 | ||||
| chr12:47758173-47758284 | Common:1; Rare:19 | ||||
| chr12:47758824-47759062 | Common:1; Rare:46 | ||||
| chr12:47904992-47905151 | Common:1; Rare:47; Clinvar:1 | ||||
| chr12:48004436-48004605 | Common:3; Rare:29; Clinvar (benign):2 |