| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34458522-34458812 | Common:1; Rare:73 | ||||
| chr9:34637725-34638118 | Common:3; Rare:105 | ||||
| chr9:34665386-34665628 | Rare:75 | ||||
| chr9:35489956-35490159 | Common:2; Rare:55 | ||||
| chr9:35658018-35658365 | Common:6; Rare:224; Clinvar:15; Clinvar (benign):10; Clinvar (pathogenic):24 | ||||
| chr9:35689706-35690037 | Common:3; Rare:109; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:35731949-35732751 | Common:5; Rare:215 | ||||
| chr9:35749210-35749347 | Common:1; Rare:65 | ||||
| chr9:35814984-35815279 | Rare:75 | ||||
| chr9:36036728-36036990 | Common:3; Rare:82 | ||||
| chr9:36037008-36037093 | Common:2; Rare:21 | ||||
| chr9:36190731-36191003 | Common:1; Rare:90 | ||||
| chr9:36258363-36258610 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37800690-37800894 | Common:2; Rare:71 | ||||
| chr9:37904035-37904247 | Common:2; Rare:64 |