| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120302037-120302372 | Rare:64 | ||||
| chr12:120361744-120362055 | Rare:67 | ||||
| chr12:120368849-120369339 | Common:4; Rare:111 | ||||
| chr12:120437933-120438151 | Common:2; Rare:78; Clinvar (benign):1 | ||||
| chr12:120446310-120446521 | Common:2; Rare:89 | ||||
| chr12:120446675-120446736 | Common:1; Rare:25 | ||||
| chr12:120446882-120446995 | Rare:17 | ||||
| chr12:120469120-120469483 | Common:3; Rare:116 | ||||
| chr12:120469484-120469923 | Common:5; Rare:150 | ||||
| chr12:120495858-120496214 | Common:7; Rare:124 | ||||
| chr12:120529082-120529397 | Common:2; Rare:92 | ||||
| chr12:120529402-120529498 | Common:1; Rare:15 | ||||
| chr12:120534172-120534441 | Common:2; Rare:72 | ||||
| chr12:120534784-120534834 | Rare:20 | ||||
| chr12:120534853-120534883 | Rare:14 |