| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34652105-34652223 | Rare:39 | ||||
| chr9:34665373-34665660 | Rare:94 | ||||
| chr9:35161860-35162059 | Common:3; Rare:57 | ||||
| chr9:35657857-35657891 | Common:1; Rare:29; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr9:35657893-35658456 | Common:8; Rare:436; Clinvar:34; Clinvar (benign):13; Clinvar (pathogenic):37 | ||||
| chr9:35685267-35685554 | Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:35689702-35690123 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35703585-35703784 | Rare:50 | ||||
| chr9:35732073-35732334 | Common:2; Rare:70 | ||||
| chr9:35732368-35732775 | Common:4; Rare:103 | ||||
| chr9:35748912-35749362 | Common:3; Rare:155 | ||||
| chr9:35814975-35815293 | Rare:80 | ||||
| chr9:35829028-35829275 | Common:3; Rare:63 | ||||
| chr9:36190703-36190982 | Common:1; Rare:96 | ||||
| chr9:36258386-36258607 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):1 |