| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120532539-120532709 | Rare:38 | ||||
| chr9:120580118-120580386 | Common:1; Rare:83; Clinvar:5 | ||||
| chr9:120714452-120714706 | Common:2; Rare:81 | ||||
| chr9:120793242-120793534 | Common:1; Rare:105 | ||||
| chr9:120842905-120843089 | Common:1; Rare:65 | ||||
| chr9:120929132-120929148 | Common:1; Rare:2 | ||||
| chr9:120929152-120929181 | Rare:9 | ||||
| chr9:121050188-121050624 | Rare:101; Clinvar (pathogenic):1 | ||||
| chr9:121074849-121074976 | Rare:61 | ||||
| chr9:121201832-121202179 | Common:2; Rare:100 | ||||
| chr9:121325938-121326427 | Common:4; Rare:86 | ||||
| chr9:121326576-121326791 | Common:2; Rare:86; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:121327076-121327435 | Common:6; Rare:101; Clinvar (benign):2 | ||||
| chr9:121328928-121329315 | Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:121370179-121370529 | Common:2; Rare:103 |