| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33264622-33265146 | Common:1; Rare:156 | ||||
| chr9:34048827-34048991 | Common:2; Rare:73 | ||||
| chr9:34049188-34049293 | Common:1; Rare:26 | ||||
| chr9:34178973-34179085 | Common:1; Rare:34 | ||||
| chr9:34329241-34329591 | Rare:101 | ||||
| chr9:34637725-34638125 | Common:3; Rare:105 | ||||
| chr9:35057145-35057532 | Rare:88; Clinvar (benign):3 | ||||
| chr9:35658016-35658337 | Common:6; Rare:224; Clinvar:16; Clinvar (benign):10; Clinvar (pathogenic):29 | ||||
| chr9:35689861-35690111 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:35732084-35732356 | Common:1; Rare:83 | ||||
| chr9:35732372-35732683 | Common:3; Rare:78 | ||||
| chr9:35748965-35749316 | Common:2; Rare:118 | ||||
| chr9:35814984-35815321 | Common:1; Rare:87 | ||||
| chr9:37800689-37800903 | Common:2; Rare:72 | ||||
| chr9:37904063-37904441 | Common:3; Rare:126 |