| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121299605-121300026 | Common:5; Rare:135; Clinvar:3 | ||||
| chr9:121326403-121326710 | Common:4; Rare:101; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:121328921-121329315 | Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:121370172-121370541 | Common:2; Rare:107 | ||||
| chr9:122159731-122159933 | Rare:66 | ||||
| chr9:122264577-122264691 | Common:2; Rare:28 | ||||
| chr9:122264762-122264922 | Common:2; Rare:48 | ||||
| chr9:122905257-122905598 | Common:2; Rare:121 | ||||
| chr9:122913293-122913417 | Common:1; Rare:26 | ||||
| chr9:122931482-122931684 | Common:3; Rare:39 | ||||
| chr9:124861908-124862113 | Rare:88 | ||||
| chr9:124940969-124941156 | Common:3; Rare:62 | ||||
| chr9:125189722-125190029 | Common:1; Rare:141 | ||||
| chr9:125200448-125200590 | Rare:54 | ||||
| chr9:125241317-125241656 | Common:2; Rare:99 |