| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53306042-53306250 | Rare:61 | ||||
| chr12:53321228-53321414 | Common:1; Rare:65; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53500162-53500255 | Rare:15 | ||||
| chr12:53501209-53501357 | Rare:36 | ||||
| chr12:53501513-53501606 | Rare:22 | ||||
| chr12:53625936-53626125 | Common:1; Rare:47 | ||||
| chr12:53626327-53626557 | Common:3; Rare:58 | ||||
| chr12:53676057-53676416 | Common:3; Rare:156 | ||||
| chr12:53727403-53727779 | Rare:80 | ||||
| chr12:53999957-54000147 | Common:4; Rare:52 | ||||
| chr12:54009552-54009712 | Common:1; Rare:56 | ||||
| chr12:54028355-54028473 | Rare:28 | ||||
| chr12:54053777-54053915 | Rare:25 | ||||
| chr12:54259525-54259724 | Rare:38 | ||||
| chr12:54280021-54280297 | Rare:92 |