| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123268216-123268326 | Rare:14 | ||||
| chr12:123364820-123364934 | Common:1; Rare:44 | ||||
| chr12:123584325-123584616 | Common:5; Rare:100 | ||||
| chr12:123602030-123602184 | Common:3; Rare:56 | ||||
| chr12:123633617-123633851 | Common:1; Rare:110; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972993-123973294 | Common:2; Rare:92 | ||||
| chr12:124863833-124864114 | Common:1; Rare:77 | ||||
| chr12:124914585-124914985 | Common:8; Rare:155 | ||||
| chr12:130716260-130716345 | Rare:13 | ||||
| chr12:130839151-130839354 | Common:2; Rare:80 | ||||
| chr12:130871759-130872110 | Common:4; Rare:141 | ||||
| chr12:131710843-131711118 | Rare:66 | ||||
| chr12:132687311-132687656 | Common:2; Rare:129; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710751-132710993 | Common:3; Rare:81 | ||||
| chr12:132828820-132829159 | Common:4; Rare:115 |