| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19127467-19127556 | Common:1; Rare:23 | ||||
| chr9:19380196-19380360 | Common:4; Rare:82 | ||||
| chr9:20684058-20684282 | Common:3; Rare:90 | ||||
| chr9:21802515-21802677 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:26892738-26892858 | Rare:65 | ||||
| chr9:26947139-26947312 | Rare:56 | ||||
| chr9:27573732-27573944 | Common:2; Rare:66; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:33001547-33001769 | Common:3; Rare:107; Clinvar (benign):4 | ||||
| chr9:33025081-33025383 | Common:7; Rare:125 | ||||
| chr9:33076619-33076880 | Common:2; Rare:89 | ||||
| chr9:33166862-33166956 | Rare:38 | ||||
| chr9:33290363-33290575 | Common:2; Rare:81 | ||||
| chr9:34126631-34126855 | Common:1; Rare:64 | ||||
| chr9:34329210-34329606 | Rare:124 | ||||
| chr9:34612084-34612338 | Common:9; Rare:80 |