| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118372846-118373171 | Common:2; Rare:86 | ||||
| chr12:119178615-119178976 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119668038-119668203 | Common:1; Rare:40 | ||||
| chr12:120116607-120116949 | Common:5; Rare:97 | ||||
| chr12:120201081-120201360 | Common:2; Rare:89 | ||||
| chr12:120438047-120438395 | Common:1; Rare:134; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446284-120446483 | Common:1; Rare:78 | ||||
| chr12:120469437-120470042 | Common:7; Rare:184 | ||||
| chr12:120495845-120496304 | Common:7; Rare:153 | ||||
| chr12:120581344-120581538 | Common:1; Rare:70 | ||||
| chr12:120686971-120687171 | Common:1; Rare:67 | ||||
| chr12:120903435-120903634 | Rare:39 | ||||
| chr12:121399869-121400189 | Common:5; Rare:118 | ||||
| chr12:121800020-121800181 | Common:2; Rare:35 | ||||
| chr12:121802915-121803091 | Rare:44 |