| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53999988-54000250 | Common:3; Rare:71 | ||||
| chr12:54016807-54017205 | Common:1; Rare:86 | ||||
| chr12:54283779-54283851 | Rare:27; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:54283853-54284168 | Common:1; Rare:71; Clinvar (pathogenic):3 | ||||
| chr12:54391240-54391391 | Rare:33 | ||||
| chr12:54419160-54419350 | Rare:56 | ||||
| chr12:55726666-55727341 | Common:4; Rare:217 | ||||
| chr12:55728271-55728482 | Rare:74 | ||||
| chr12:55728883-55729146 | Common:2; Rare:51 | ||||
| chr12:55729256-55729794 | Common:2; Rare:112 | ||||
| chr12:55818735-55819077 | Rare:79 | ||||
| chr12:55829473-55829824 | Rare:110 | ||||
| chr12:55830221-55830249 | Rare:3 | ||||
| chr12:55830744-55830943 | Rare:64 | ||||
| chr12:55927742-55927790 | Rare:16 |