| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35161819-35162141 | Common:4; Rare:92 | ||||
| chr9:35489922-35490139 | Common:2; Rare:61 | ||||
| chr9:35657850-35658386 | Common:8; Rare:444; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35703829-35704053 | Common:1; Rare:66 | ||||
| chr9:35732074-35732320 | Common:1; Rare:66 | ||||
| chr9:35732365-35732722 | Common:3; Rare:89 | ||||
| chr9:35748876-35749395 | Common:3; Rare:170 | ||||
| chr9:35814978-35815294 | Rare:79 | ||||
| chr9:36190690-36190989 | Common:1; Rare:101 | ||||
| chr9:36191084-36191273 | Common:1; Rare:51 | ||||
| chr9:36258395-36258622 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400841-36400975 | Common:3; Rare:63 | ||||
| chr9:37422560-37422752 | Common:2; Rare:97 | ||||
| chr9:37592483-37592648 | Common:2; Rare:65 | ||||
| chr9:37785006-37785174 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):3 |