| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53307166-53307476 | Common:3; Rare:71; Clinvar (benign):1 | ||||
| chr12:53939491-53939573 | Rare:27 | ||||
| chr12:53939576-53939692 | Common:1; Rare:32 | ||||
| chr12:53939754-53939792 | Rare:10 | ||||
| chr12:53973698-53973826 | Rare:46 | ||||
| chr12:53974632-53974750 | Rare:23 | ||||
| chr12:54049226-54049525 | Common:2; Rare:68 | ||||
| chr12:54126492-54126586 | Rare:23 | ||||
| chr12:54128647-54128982 | Common:2; Rare:46 | ||||
| chr12:54282703-54282874 | Rare:52 | ||||
| chr12:54370407-54370661 | Common:2; Rare:69 | ||||
| chr12:54936903-54937036 | Common:2; Rare:24 | ||||
| chr12:55831521-55831830 | Rare:46 | ||||
| chr12:55832149-55832360 | Rare:43 | ||||
| chr12:55833513-55833587 | Rare:11 |