| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120842905-120843111 | Common:1; Rare:73 | ||||
| chr9:121201838-121202172 | Common:2; Rare:93 | ||||
| chr9:121268058-121268207 | Common:1; Rare:48 | ||||
| chr9:122159708-122159911 | Rare:77 | ||||
| chr9:122264762-122264916 | Common:2; Rare:47 | ||||
| chr9:122913282-122913395 | Common:1; Rare:23 | ||||
| chr9:124940969-124941152 | Common:3; Rare:62 | ||||
| chr9:125189744-125190029 | Common:1; Rare:123 | ||||
| chr9:125200482-125200590 | Rare:40 | ||||
| chr9:125261680-125261834 | Common:1; Rare:61 | ||||
| chr9:127451282-127451520 | Common:2; Rare:105 | ||||
| chr9:127829660-127829703 | Common:1; Rare:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:127854572-127854877 | Rare:67; Clinvar:6 | ||||
| chr9:127877666-127877771 | Rare:20 | ||||
| chr9:128098289-128098537 | Common:1; Rare:52 |