| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97012554-97012875 | Common:4; Rare:66 | ||||
| chr9:97238263-97238492 | Common:4; Rare:71 | ||||
| chr9:97786463-97786641 | Rare:34 | ||||
| chr9:98944276-98944464 | Rare:38 | ||||
| chr9:111039198-111039439 | Common:2; Rare:50 | ||||
| chr9:111897942-111898086 | Common:3; Rare:23 | ||||
| chr9:116838200-116838472 | Common:4; Rare:51 | ||||
| chr9:121318436-121318873 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:121324313-121324626 | Common:1; Rare:69 | ||||
| chr9:121498588-121498606 | Rare:6 | ||||
| chr9:121499670-121499827 | Rare:49 | ||||
| chr9:122369742-122369942 | Common:2; Rare:44 | ||||
| chr9:124658174-124658436 | Rare:46 | ||||
| chr9:125153618-125153951 | Common:2; Rare:64 | ||||
| chr9:127509106-127509148 | Rare:14 |