| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51391603-51391792 | Common:2; Rare:58 | ||||
| chr12:52055830-52056086 | Common:4; Rare:75 | ||||
| chr12:52070158-52070388 | Rare:57 | ||||
| chr12:52948803-52949093 | Common:2; Rare:63 | ||||
| chr12:53006133-53006494 | Common:4; Rare:128 | ||||
| chr12:53047006-53047046 | Rare:10 | ||||
| chr12:53049018-53049224 | Common:1; Rare:56 | ||||
| chr12:53049720-53050175 | Common:1; Rare:114 | ||||
| chr12:53103446-53103566 | Common:1; Rare:21 | ||||
| chr12:53180548-53180573 | Rare:11 | ||||
| chr12:53180585-53180794 | Common:1; Rare:81 | ||||
| chr12:53252038-53252217 | Common:3; Rare:68 | ||||
| chr12:53295430-53295638 | Common:1; Rare:70 | ||||
| chr12:53321240-53321413 | Common:1; Rare:63; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53381510-53381809 | Rare:95 |