| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:114683945-114684069 | Rare:23 | ||||
| chr12:114684125-114684353 | Rare:62 | ||||
| chr12:114684493-114684652 | Rare:43 | ||||
| chr12:118061059-118061407 | Common:3; Rare:80 | ||||
| chr12:118103876-118104128 | Common:1; Rare:60 | ||||
| chr12:118135929-118136224 | Common:2; Rare:93 | ||||
| chr12:118372827-118373165 | Common:2; Rare:88 | ||||
| chr12:119178689-119178948 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:120116715-120116955 | Common:2; Rare:86 | ||||
| chr12:120194697-120194798 | Rare:38 | ||||
| chr12:120201081-120201372 | Common:2; Rare:91 | ||||
| chr12:120446344-120446474 | Common:1; Rare:58 | ||||
| chr12:120469476-120469895 | Common:5; Rare:140 | ||||
| chr12:120495871-120496158 | Common:6; Rare:96 | ||||
| chr12:120686967-120687171 | Common:1; Rare:71 |