| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120686727-120686882 | Rare:34 | ||||
| chr12:120686904-120687291 | Common:2; Rare:125 | ||||
| chr12:120687344-120687501 | Rare:42 | ||||
| chr12:120710349-120710562 | Common:2; Rare:79 | ||||
| chr12:120710634-120710996 | Common:1; Rare:87 | ||||
| chr12:120725668-120725890 | Common:3; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:120903378-120903792 | Common:3; Rare:104 | ||||
| chr12:120904078-120904189 | Common:1; Rare:29 | ||||
| chr12:120904268-120904521 | Common:3; Rare:98 | ||||
| chr12:121016348-121016591 | Common:5; Rare:105 | ||||
| chr12:121038969-121039146 | Common:2; Rare:38 | ||||
| chr12:121133286-121133514 | Common:1; Rare:51 | ||||
| chr12:121209905-121210529 | Common:7; Rare:198 | ||||
| chr12:121296340-121296427 | Rare:13 | ||||
| chr12:121296602-121297058 | Common:3; Rare:128 |