| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35665172-35665317 | Common:2; Rare:54 | ||||
| chr9:35685433-35685783 | Common:1; Rare:80; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:35689704-35690123 | Common:4; Rare:130; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35691063-35691328 | Common:1; Rare:57 | ||||
| chr9:35698808-35699185 | Common:1; Rare:103 | ||||
| chr9:35732078-35732361 | Common:2; Rare:85 | ||||
| chr9:35732366-35732718 | Common:3; Rare:89 | ||||
| chr9:35748891-35749379 | Common:3; Rare:162 | ||||
| chr9:35814901-35815302 | Rare:109 | ||||
| chr9:36190763-36191149 | Common:1; Rare:125 | ||||
| chr9:36400926-36401303 | Common:3; Rare:126 | ||||
| chr9:36572742-36573027 | Common:2; Rare:80 | ||||
| chr9:37422580-37422773 | Common:2; Rare:96; Clinvar:1 | ||||
| chr9:37784703-37784815 | Rare:41; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr9:37784875-37785108 | Common:1; Rare:113; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):3 |