| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127877638-127877791 | Rare:36 | ||||
| chr9:127897406-127897560 | Common:1; Rare:42 | ||||
| chr9:127899518-127899742 | Rare:81 | ||||
| chr9:127916982-127917304 | Common:1; Rare:95 | ||||
| chr9:127937816-127937926 | Common:1; Rare:32; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:128098442-128098544 | Common:1; Rare:21 | ||||
| chr9:128128365-128128494 | Common:1; Rare:49 | ||||
| chr9:128149264-128149436 | Rare:28 | ||||
| chr9:128151633-128152294 | Common:3; Rare:207; Clinvar (benign):1 | ||||
| chr9:128190391-128190710 | Rare:84 | ||||
| chr9:128191515-128191651 | Rare:35 | ||||
| chr9:128275900-128276312 | Common:5; Rare:181 | ||||
| chr9:128322366-128322621 | Common:1; Rare:87 | ||||
| chr9:128322739-128322918 | Common:3; Rare:85; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:128340164-128340180 | Rare:9 |