| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120842897-120843251 | Common:1; Rare:116 | ||||
| chr9:121074851-121074977 | Rare:61 | ||||
| chr9:121075074-121075349 | Rare:66 | ||||
| chr9:121201829-121201915 | Rare:32 | ||||
| chr9:121268063-121268207 | Common:1; Rare:48 | ||||
| chr9:121285940-121286146 | Common:1; Rare:47 | ||||
| chr9:121286961-121287146 | Common:1; Rare:47 | ||||
| chr9:121327011-121327482 | Common:6; Rare:123; Clinvar (benign):2 | ||||
| chr9:121328804-121329315 | Common:2; Rare:141; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:121370172-121370458 | Common:2; Rare:82 | ||||
| chr9:121566943-121567123 | Rare:41 | ||||
| chr9:122159731-122159924 | Rare:60 | ||||
| chr9:122264332-122264691 | Common:3; Rare:73 | ||||
| chr9:122264768-122264922 | Common:2; Rare:46 | ||||
| chr9:122913278-122913431 | Common:3; Rare:36 |