| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53180905-53181150 | Common:4; Rare:67 | ||||
| chr12:53232186-53232433 | Common:2; Rare:54 | ||||
| chr12:53252046-53252212 | Common:3; Rare:64 | ||||
| chr12:53321240-53321429 | Common:1; Rare:70; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:53321514-53321652 | Common:1; Rare:41; Clinvar:3 | ||||
| chr12:53501209-53501357 | Rare:36 | ||||
| chr12:53501524-53501621 | Rare:23 | ||||
| chr12:53625942-53626137 | Common:1; Rare:47 | ||||
| chr12:53676057-53676383 | Common:3; Rare:149 | ||||
| chr12:54028228-54028456 | Common:6; Rare:67 | ||||
| chr12:54259526-54259738 | Rare:39 | ||||
| chr12:54391253-54391466 | Rare:50 | ||||
| chr12:54419196-54419441 | Common:1; Rare:66 | ||||
| chr12:54419453-54419657 | Rare:35 | ||||
| chr12:55716010-55716195 | Common:1; Rare:87 |