| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111599275-111599679 | Common:3; Rare:145 | ||||
| chr12:111685894-111686133 | Rare:87 | ||||
| chr12:111715190-111715680 | Common:2; Rare:81 | ||||
| chr12:111766844-111766968 | Rare:38 | ||||
| chr12:111841845-111842301 | Common:3; Rare:132 | ||||
| chr12:111842487-111842887 | Common:1; Rare:162 | ||||
| chr12:112012499-112012899 | Common:1; Rare:96 | ||||
| chr12:112013119-112013492 | Common:1; Rare:138 | ||||
| chr12:112108749-112108993 | Common:1; Rare:60 | ||||
| chr12:112125325-112125592 | Rare:67 | ||||
| chr12:112381200-112382180 | Common:1; Rare:246 | ||||
| chr12:112382363-112382603 | Common:1; Rare:79 | ||||
| chr12:112409553-112409710 | Common:1; Rare:52 | ||||
| chr12:112418807-112418983 | Common:1; Rare:56; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:113056660-113056931 | Common:2; Rare:77 |