| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:16573780-16573972 | Rare:41 | ||||
| chr12:16574472-16574726 | Common:1; Rare:40 | ||||
| chr12:16576423-16576734 | Common:1; Rare:54 | ||||
| chr12:16588930-16589052 | Common:2; Rare:18 | ||||
| chr12:16589089-16589129 | Rare:7 | ||||
| chr12:16591272-16591510 | Rare:35 | ||||
| chr12:16596930-16596991 | Rare:7 | ||||
| chr12:21474925-21475153 | Rare:66; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:21662588-21662703 | Common:4; Rare:50 | ||||
| chr12:21817279-21817365 | Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:21829031-21829265 | Common:5; Rare:63; Clinvar:6; Clinvar (benign):1 | ||||
| chr12:24562096-24562283 | Common:3; Rare:36 | ||||
| chr12:25386189-25386370 | Rare:70 | ||||
| chr12:29158499-29158540 | Rare:5 | ||||
| chr12:40156466-40156647 | Common:1; Rare:30 |