| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50025372-50025811 | Common:2; Rare:119 | ||||
| chr12:50084997-50085415 | Common:1; Rare:110 | ||||
| chr12:50085434-50085683 | Rare:55 | ||||
| chr12:50111633-50112326 | Common:2; Rare:152; Clinvar (benign):1 | ||||
| chr12:50112395-50112438 | Rare:6 | ||||
| chr12:50166917-50167140 | Rare:51 | ||||
| chr12:50167223-50167735 | Common:4; Rare:133 | ||||
| chr12:50220572-50220895 | Common:1; Rare:48 | ||||
| chr12:50222261-50222469 | Rare:57 | ||||
| chr12:50222590-50222752 | Rare:29 | ||||
| chr12:50283476-50283761 | Common:4; Rare:84 | ||||
| chr12:50400667-50401214 | Common:1; Rare:158 | ||||
| chr12:50401289-50401448 | Common:1; Rare:36 | ||||
| chr12:50504826-50505169 | Common:4; Rare:136 | ||||
| chr12:50763439-50763544 | Common:3; Rare:16 |