| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64222242-64222333 | Rare:32 | ||||
| chr12:64404178-64404572 | Common:4; Rare:146 | ||||
| chr12:64452025-64452163 | Common:1; Rare:52 | ||||
| chr12:64759373-64759501 | Common:1; Rare:42; Clinvar:3 | ||||
| chr12:65169451-65169618 | Common:1; Rare:60; Clinvar:2 | ||||
| chr12:65278646-65278764 | Rare:37 | ||||
| chr12:65278816-65278997 | Rare:50; Clinvar (benign):2 | ||||
| chr12:65279022-65279143 | Rare:29 | ||||
| chr12:65279331-65279461 | Common:1; Rare:39 | ||||
| chr12:65824895-65825122 | Common:1; Rare:54 | ||||
| chr12:66130705-66130861 | Rare:56 | ||||
| chr12:66169921-66170106 | Common:1; Rare:55 | ||||
| chr12:67269139-67269527 | Common:3; Rare:109 | ||||
| chr12:67269541-67269662 | Rare:39 | ||||
| chr12:68332250-68332631 | Common:1; Rare:130 |