| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120843302-120843450 | Rare:33 | ||||
| chr9:120868827-120869069 | Common:2; Rare:51 | ||||
| chr9:120877157-120877456 | Common:3; Rare:95 | ||||
| chr9:120929123-120929238 | Common:3; Rare:28 | ||||
| chr9:121074829-121074973 | Rare:69 | ||||
| chr9:121201814-121202188 | Common:2; Rare:113 | ||||
| chr9:121268040-121268213 | Common:1; Rare:61 | ||||
| chr9:121285871-121286146 | Common:1; Rare:59 | ||||
| chr9:121328890-121329315 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:121370184-121370545 | Common:2; Rare:107 | ||||
| chr9:122092856-122093004 | Common:2; Rare:47 | ||||
| chr9:122093302-122093485 | Common:1; Rare:76 | ||||
| chr9:122159716-122159919 | Rare:72 | ||||
| chr9:122264577-122264663 | Common:1; Rare:20 | ||||
| chr9:122264721-122264925 | Common:2; Rare:57 |