| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35689697-35690123 | Common:4; Rare:132; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35732073-35732320 | Common:1; Rare:66 | ||||
| chr9:35732373-35732718 | Common:3; Rare:86 | ||||
| chr9:35748989-35749369 | Common:2; Rare:141 | ||||
| chr9:35814983-35815293 | Rare:79 | ||||
| chr9:36190718-36191068 | Common:2; Rare:108 | ||||
| chr9:36258395-36258625 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37800707-37800788 | Rare:23 | ||||
| chr9:37904067-37904222 | Rare:52 | ||||
| chr9:68779966-68780094 | Common:1; Rare:42 | ||||
| chr9:69759934-69760123 | Common:2; Rare:87 | ||||
| chr9:70258829-70259069 | Common:4; Rare:114 | ||||
| chr9:70413944-70414192 | Rare:48 | ||||
| chr9:70414309-70414511 | Rare:47 | ||||
| chr9:71911192-71911514 | Common:3; Rare:93 |