| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121626322-121626872 | Common:3; Rare:233; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:121626880-121626930 | Common:2; Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:121626976-121627188 | Rare:78; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:121627194-121627372 | Common:2; Rare:28 | ||||
| chr12:121672564-121672722 | Common:4; Rare:46 | ||||
| chr12:121712410-121712860 | Common:6; Rare:134 | ||||
| chr12:121793625-121793731 | Common:1; Rare:40 | ||||
| chr12:121794238-121794466 | Common:1; Rare:66 | ||||
| chr12:121802893-121803159 | Common:1; Rare:71 | ||||
| chr12:121803161-121803392 | Rare:60 | ||||
| chr12:121803395-121803740 | Common:1; Rare:89 | ||||
| chr12:121803836-121804407 | Rare:193 | ||||
| chr12:121804737-121804749 | Rare:2 | ||||
| chr12:121888360-121888925 | Common:3; Rare:150 | ||||
| chr12:121889031-121889199 | Rare:33 |