| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:21031430-21031567 | Common:2; Rare:50 | ||||
| chr9:21031602-21031700 | Common:1; Rare:39 | ||||
| chr9:21802323-21802692 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:25677975-25678401 | Common:4; Rare:166 | ||||
| chr9:26892319-26892887 | Common:2; Rare:271 | ||||
| chr9:26947024-26947299 | Common:1; Rare:102 | ||||
| chr9:26947366-26947566 | Common:1; Rare:67 | ||||
| chr9:26956214-26956464 | Common:2; Rare:89 | ||||
| chr9:27529618-27529656 | Rare:5 | ||||
| chr9:27529709-27529835 | Common:3; Rare:40 | ||||
| chr9:27573403-27573555 | Common:6; Rare:92 | ||||
| chr9:27573716-27573980 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384512-32384731 | Common:1; Rare:83 | ||||
| chr9:32552557-32552633 | Common:1; Rare:14; Clinvar:2 | ||||
| chr9:32573058-32573235 | Common:3; Rare:65 |