| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35657881-35658376 | Common:7; Rare:411; Clinvar:35; Clinvar (benign):14; Clinvar (pathogenic):37 | ||||
| chr9:35732091-35732212 | Rare:39 | ||||
| chr9:35732373-35732679 | Common:3; Rare:77 | ||||
| chr9:35748989-35749352 | Common:2; Rare:136 | ||||
| chr9:36190697-36190973 | Common:1; Rare:95 | ||||
| chr9:36572753-36572902 | Common:1; Rare:47 | ||||
| chr9:37422613-37422749 | Common:2; Rare:73 | ||||
| chr9:37485794-37485996 | Rare:77 | ||||
| chr9:37904103-37904222 | Rare:36 | ||||
| chr9:70258824-70259069 | Common:4; Rare:117 | ||||
| chr9:71768510-71768602 | Rare:21 | ||||
| chr9:75088177-75088526 | Common:3; Rare:119 | ||||
| chr9:78296878-78297138 | Common:1; Rare:67 | ||||
| chr9:83707683-83708295 | Common:5; Rare:201 | ||||
| chr9:83979619-83979745 | Rare:36 |