| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:126860558-126860705 | Common:2; Rare:49 | ||||
| chr9:127122662-127122994 | Common:3; Rare:91 | ||||
| chr9:127224379-127224652 | Rare:74 | ||||
| chr9:127245161-127245341 | Common:1; Rare:42 | ||||
| chr9:127398088-127398198 | Common:1; Rare:27 | ||||
| chr9:127424071-127424537 | Common:1; Rare:134 | ||||
| chr9:127451274-127451565 | Common:3; Rare:120; Clinvar (benign):1 | ||||
| chr9:127612017-127612378 | Common:2; Rare:130; Clinvar:4; Clinvar (benign):3 | ||||
| chr9:127706952-127707028 | Rare:29 | ||||
| chr9:127735273-127735578 | Common:1; Rare:77 | ||||
| chr9:127771286-127771363 | Rare:24 | ||||
| chr9:127802592-127803032 | Common:3; Rare:118 | ||||
| chr9:127824889-127825189 | Rare:73; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:127854490-127854574 | Rare:20; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:127873477-127873618 | Common:1; Rare:33 |