| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34329186-34329598 | Rare:131 | ||||
| chr9:34458540-34458847 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:34665373-34665660 | Rare:94 | ||||
| chr9:35657850-35658397 | Common:9; Rare:451; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35689702-35689969 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35689971-35690157 | Common:1; Rare:52; Clinvar:2 | ||||
| chr9:35732089-35732320 | Rare:66 | ||||
| chr9:35732373-35732676 | Common:2; Rare:76 | ||||
| chr9:35748987-35749357 | Common:2; Rare:139 | ||||
| chr9:35814982-35815293 | Rare:79 | ||||
| chr9:36036852-36036980 | Common:2; Rare:47 | ||||
| chr9:36190690-36191053 | Common:2; Rare:117 | ||||
| chr9:37485764-37486006 | Rare:90 | ||||
| chr9:37904086-37904237 | Common:2; Rare:44 | ||||
| chr9:38392551-38392780 | Common:2; Rare:67 |