| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52680119-52680249 | Rare:37; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:52948819-52949157 | Common:2; Rare:84 | ||||
| chr12:52949783-52950044 | Rare:56 | ||||
| chr12:52951590-52951786 | Rare:52; Clinvar:2 | ||||
| chr12:53006049-53006489 | Common:4; Rare:157 | ||||
| chr12:53079315-53079537 | Common:2; Rare:75 | ||||
| chr12:53097491-53097701 | Rare:51 | ||||
| chr12:53180584-53180750 | Common:1; Rare:67 | ||||
| chr12:53181308-53181538 | Rare:60 | ||||
| chr12:53252049-53252220 | Common:3; Rare:65 | ||||
| chr12:53295328-53295618 | Common:2; Rare:95 | ||||
| chr12:53299353-53299816 | Common:4; Rare:169 | ||||
| chr12:53299904-53299986 | Rare:36 | ||||
| chr12:53321107-53321364 | Common:1; Rare:62 | ||||
| chr12:53441493-53441798 | Common:1; Rare:84 |