| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50166597-50166835 | Common:1; Rare:44 | ||||
| chr12:50167252-50167728 | Common:3; Rare:126 | ||||
| chr12:50283432-50283625 | Rare:55 | ||||
| chr12:50400741-50401003 | Common:1; Rare:84 | ||||
| chr12:50401309-50401455 | Common:1; Rare:35 | ||||
| chr12:50504960-50505111 | Common:2; Rare:77 | ||||
| chr12:50763913-50764501 | Common:3; Rare:170 | ||||
| chr12:51026206-51026495 | Common:4; Rare:121; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51048200-51048371 | Common:1; Rare:78 | ||||
| chr12:51083587-51083741 | Rare:50 | ||||
| chr12:51172709-51172922 | Common:3; Rare:44 | ||||
| chr12:51172924-51173247 | Rare:67 | ||||
| chr12:51238663-51238919 | Common:6; Rare:110 | ||||
| chr12:51239128-51239321 | Common:2; Rare:57 | ||||
| chr12:51269927-51270132 | Common:1; Rare:95 |