| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120196933-120197008 | Rare:26 | ||||
| chr12:120198239-120198524 | Common:5; Rare:67 | ||||
| chr12:120201065-120201380 | Common:2; Rare:103 | ||||
| chr12:120224305-120224497 | Common:1; Rare:69 | ||||
| chr12:120369162-120369335 | Rare:44 | ||||
| chr12:120437842-120438139 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:120446259-120446504 | Common:2; Rare:96 | ||||
| chr12:120469596-120469882 | Common:3; Rare:101 | ||||
| chr12:120495843-120496380 | Common:8; Rare:181 | ||||
| chr12:120528939-120528968 | Rare:11 | ||||
| chr12:120528977-120529009 | Rare:10 | ||||
| chr12:120529072-120529198 | Common:2; Rare:53 | ||||
| chr12:120581314-120581574 | Common:1; Rare:96 | ||||
| chr12:120640435-120640675 | Rare:59 | ||||
| chr12:120686947-120687310 | Common:2; Rare:113 |