| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45727599-45727839 | Rare:84 | ||||
| chr12:52007845-52008133 | Common:1; Rare:58 | ||||
| chr12:52032950-52033210 | Common:1; Rare:71 | ||||
| chr12:52147301-52147551 | Common:2; Rare:60 | ||||
| chr12:52874124-52874398 | Common:10; Rare:76 | ||||
| chr12:53027765-53028185 | Common:1; Rare:146 | ||||
| chr12:53965979-53966119 | Rare:24 | ||||
| chr12:55697215-55697477 | Common:2; Rare:70; Clinvar (benign):3 | ||||
| chr12:55709758-55709985 | Common:1; Rare:32 | ||||
| chr12:55718886-55719148 | Common:1; Rare:51 | ||||
| chr12:56634993-56635100 | Rare:16 | ||||
| chr12:57143394-57143704 | Common:1; Rare:56 | ||||
| chr12:57184203-57184452 | Rare:56 | ||||
| chr12:57194124-57194391 | Common:3; Rare:71 | ||||
| chr12:57195770-57196242 | Common:3; Rare:128 |