| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120696279-120696679 | Common:2; Rare:112 | ||||
| chr12:120710182-120710970 | Common:8; Rare:389 | ||||
| chr12:120725566-120725966 | Common:12; Rare:320; Clinvar:4; Clinvar (pathogenic):4 | ||||
| chr12:120902836-120903016 | Common:2; Rare:34 | ||||
| chr12:120903210-120903951 | Common:15; Rare:410 | ||||
| chr12:120904200-120904730 | Common:16; Rare:520 | ||||
| chr12:121016339-121016739 | Common:16; Rare:328 | ||||
| chr12:121132637-121133152 | Common:4; Rare:281; Clinvar:1 | ||||
| chr12:121209912-121210710 | Common:30; Rare:753 | ||||
| chr12:121296156-121296556 | Rare:65 | ||||
| chr12:121296637-121297180 | Common:12; Rare:659 | ||||
| chr12:121297335-121297581 | Common:2; Rare:64 | ||||
| chr12:121297685-121298085 | Common:5; Rare:143 | ||||
| chr12:121351437-121351856 | Common:2; Rare:157 | ||||
| chr12:121352088-121353069 | Common:40; Rare:1225 |