| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52948787-52949300 | Common:2; Rare:144; Clinvar:1 | ||||
| chr12:52949792-52950019 | Rare:52 | ||||
| chr12:52951477-52951856 | Rare:102; Clinvar:5 | ||||
| chr12:53006140-53006485 | Common:4; Rare:124 | ||||
| chr12:53048847-53049238 | Common:1; Rare:81 | ||||
| chr12:53049679-53050094 | Common:1; Rare:92 | ||||
| chr12:53079329-53079550 | Common:2; Rare:78 | ||||
| chr12:53170306-53170588 | Common:2; Rare:72 | ||||
| chr12:53180590-53180730 | Common:1; Rare:52 | ||||
| chr12:53252049-53252212 | Common:3; Rare:62 | ||||
| chr12:53321240-53321437 | Common:1; Rare:75; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:53441482-53441777 | Common:1; Rare:79 | ||||
| chr12:53501213-53501320 | Rare:29 | ||||
| chr12:53501490-53501614 | Rare:34 | ||||
| chr12:53727406-53727768 | Rare:79 |