| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37422461-37422753 | Common:7; Rare:121 | ||||
| chr9:37485737-37486024 | Common:3; Rare:102 | ||||
| chr9:37784996-37785086 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800518-37800816 | Common:4; Rare:90 | ||||
| chr9:37904066-37904234 | Rare:56 | ||||
| chr9:68779902-68780079 | Common:2; Rare:63 | ||||
| chr9:69759910-69760174 | Common:3; Rare:110 | ||||
| chr9:70258875-70259077 | Common:1; Rare:91 | ||||
| chr9:71911184-71911508 | Common:3; Rare:93 | ||||
| chr9:75088140-75088598 | Common:3; Rare:159 | ||||
| chr9:76459057-76459255 | Common:1; Rare:71 | ||||
| chr9:77177468-77177770 | Common:2; Rare:92; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:78296871-78297247 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr9:81687819-81687929 | Rare:44 | ||||
| chr9:81689398-81689834 | Common:11; Rare:169 |