| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125189723-125190029 | Common:1; Rare:141 | ||||
| chr9:125200421-125200590 | Common:1; Rare:64 | ||||
| chr9:125241292-125241649 | Common:2; Rare:107 | ||||
| chr9:127122606-127122949 | Common:3; Rare:88 | ||||
| chr9:127424106-127424419 | Rare:87 | ||||
| chr9:127449614-127450003 | Rare:100 | ||||
| chr9:127451261-127451562 | Common:3; Rare:124; Clinvar (benign):1 | ||||
| chr9:127473624-127473860 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:127579018-127579305 | Common:4; Rare:59 | ||||
| chr9:127899518-127899716 | Rare:71 | ||||
| chr9:127916989-127917277 | Common:1; Rare:84 | ||||
| chr9:127937832-127937906 | Common:1; Rare:19 | ||||
| chr9:128191515-128191673 | Rare:41 | ||||
| chr9:128204217-128204541 | Common:2; Rare:63 | ||||
| chr9:128260732-128260920 | Common:3; Rare:47 |