| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35162286-35162325 | Rare:10 | ||||
| chr9:35657835-35658342 | Common:10; Rare:431; Clinvar:44; Clinvar (benign):17; Clinvar (pathogenic):40 | ||||
| chr9:35732073-35732334 | Common:2; Rare:70 | ||||
| chr9:35732368-35732877 | Common:4; Rare:126 | ||||
| chr9:35737878-35738190 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35744292-35744510 | Rare:53; Clinvar:3 | ||||
| chr9:35748486-35748851 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:35748859-35749402 | Common:3; Rare:177 | ||||
| chr9:35814984-35815293 | Rare:79 | ||||
| chr9:35905945-35906260 | Common:1; Rare:76 | ||||
| chr9:36190701-36191169 | Common:3; Rare:155 | ||||
| chr9:36258386-36258607 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37784884-37785155 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr9:37800707-37800816 | Rare:30 | ||||
| chr9:37903904-37904453 | Common:4; Rare:182 |