| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12266947-12267129 | Common:3; Rare:82 | ||||
| chr12:12356986-12357220 | Common:4; Rare:115 | ||||
| chr12:12561131-12561246 | Common:1; Rare:17 | ||||
| chr12:12562236-12562319 | Rare:22 | ||||
| chr12:12562597-12562992 | Common:2; Rare:117 | ||||
| chr12:12611633-12612147 | Common:3; Rare:148 | ||||
| chr12:12684470-12684766 | Common:1; Rare:39 | ||||
| chr12:12696129-12696289 | Rare:41 | ||||
| chr12:12717244-12717434 | Rare:67; Clinvar (benign):1 | ||||
| chr12:12717589-12717769 | Common:1; Rare:48; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:12725634-12725975 | Common:4; Rare:79 | ||||
| chr12:13000249-13000472 | Common:2; Rare:64 | ||||
| chr12:13044139-13044422 | Rare:61 | ||||
| chr12:14365444-14365757 | Common:1; Rare:102 | ||||
| chr12:14567682-14567981 | Common:2; Rare:64 |