| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127122565-127122605 | Common:1; Rare:9 | ||||
| chr9:127122606-127122989 | Common:3; Rare:107 | ||||
| chr9:127224382-127224661 | Common:1; Rare:77 | ||||
| chr9:127424249-127424485 | Common:1; Rare:77 | ||||
| chr9:127449614-127449853 | Rare:60 | ||||
| chr9:127451267-127451580 | Common:3; Rare:124; Clinvar (benign):1 | ||||
| chr9:127569062-127569372 | Common:4; Rare:74 | ||||
| chr9:127612050-127612344 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127877645-127877755 | Rare:28 | ||||
| chr9:127899518-127899742 | Rare:81 | ||||
| chr9:127905250-127905436 | Common:1; Rare:32 | ||||
| chr9:127916972-127917304 | Common:1; Rare:98 | ||||
| chr9:127937824-127937913 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128098278-128098549 | Common:1; Rare:57 | ||||
| chr9:128128384-128128524 | Common:2; Rare:67 |