| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35161819-35162032 | Common:4; Rare:61 | ||||
| chr9:35489638-35490163 | Common:4; Rare:151 | ||||
| chr9:35538477-35539018 | Common:3; Rare:102 | ||||
| chr9:35657990-35658352 | Common:6; Rare:268; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):33 | ||||
| chr9:35665075-35665340 | Common:3; Rare:93 | ||||
| chr9:35673884-35673950 | Common:2; Rare:20 | ||||
| chr9:35689692-35690074 | Common:3; Rare:124; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35691078-35691235 | Common:1; Rare:34 | ||||
| chr9:35698886-35699456 | Common:1; Rare:147 | ||||
| chr9:35699490-35699882 | Common:1; Rare:71 | ||||
| chr9:35704028-35704354 | Common:2; Rare:91 | ||||
| chr9:35732074-35732718 | Common:5; Rare:176 | ||||
| chr9:35733055-35733467 | Rare:144 | ||||
| chr9:35744350-35744661 | Common:2; Rare:71; Clinvar:2 | ||||
| chr9:35748957-35749392 | Common:2; Rare:157 |