| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120248633-120248826 | Common:2; Rare:24 | ||||
| chr12:120265612-120265822 | Rare:98 | ||||
| chr12:120437804-120438140 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr12:120446229-120446491 | Common:2; Rare:97 | ||||
| chr12:120469433-120469868 | Common:5; Rare:141 | ||||
| chr12:120495843-120496236 | Common:8; Rare:131 | ||||
| chr12:120534312-120534399 | Rare:37 | ||||
| chr12:120575631-120575945 | Common:2; Rare:87 | ||||
| chr12:120581337-120581574 | Common:1; Rare:82 | ||||
| chr12:120686936-120687210 | Common:2; Rare:96 | ||||
| chr12:120687345-120687525 | Rare:46 | ||||
| chr12:120903349-120903631 | Common:2; Rare:56 | ||||
| chr12:120904258-120904493 | Common:3; Rare:92 | ||||
| chr12:121038937-121039308 | Common:3; Rare:78 | ||||
| chr12:121352138-121352254 | Rare:46 |