| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48105314-48105706 | Common:3; Rare:88 | ||||
| chr12:48105777-48106223 | Common:4; Rare:135 | ||||
| chr12:48106241-48106493 | Rare:61 | ||||
| chr12:48119147-48119369 | Common:2; Rare:44; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48156833-48157115 | Common:1; Rare:45 | ||||
| chr12:48157447-48157774 | Common:5; Rare:85 | ||||
| chr12:48682182-48682582 | Common:6; Rare:120 | ||||
| chr12:48716603-48717158 | Common:6; Rare:174 | ||||
| chr12:48717166-48717189 | Rare:6 | ||||
| chr12:48717384-48717545 | Rare:24 | ||||
| chr12:48814694-48814921 | Rare:40 | ||||
| chr12:48815353-48815574 | Common:1; Rare:52 | ||||
| chr12:48851975-48852448 | Common:3; Rare:125 | ||||
| chr12:48852726-48852779 | Rare:9 | ||||
| chr12:48853334-48853386 | Rare:12 |