| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:126860576-126860684 | Common:2; Rare:31 | ||||
| chr9:127245188-127245341 | Common:1; Rare:37 | ||||
| chr9:127424071-127424495 | Common:1; Rare:126 | ||||
| chr9:127451261-127451565 | Common:3; Rare:125; Clinvar (benign):1 | ||||
| chr9:127788326-127788692 | Common:2; Rare:128 | ||||
| chr9:127802737-127803056 | Common:4; Rare:84 | ||||
| chr9:127854372-127854447 | Common:1; Rare:23; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:127877656-127877809 | Rare:33 | ||||
| chr9:127897313-127897546 | Common:1; Rare:54 | ||||
| chr9:127899510-127899742 | Rare:83 | ||||
| chr9:127916972-127917259 | Common:1; Rare:87 | ||||
| chr9:127937824-127937923 | Common:1; Rare:27; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128098289-128098549 | Common:1; Rare:56 | ||||
| chr9:128160046-128160486 | Common:2; Rare:106 | ||||
| chr9:128169134-128169462 | Common:2; Rare:75; Clinvar (benign):1 |