| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:21802482-21802687 | Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:23826082-23826493 | Common:2; Rare:150 | ||||
| chr9:26892731-26892867 | Rare:68 | ||||
| chr9:26947146-26947273 | Rare:45 | ||||
| chr9:26956265-26956459 | Common:2; Rare:73 | ||||
| chr9:27529738-27529869 | Common:4; Rare:42 | ||||
| chr9:27573414-27573530 | Common:6; Rare:60 | ||||
| chr9:32552565-32552645 | Common:1; Rare:13; Clinvar:2 | ||||
| chr9:32573003-32573211 | Common:2; Rare:72 | ||||
| chr9:33001565-33001746 | Common:3; Rare:90; Clinvar (benign):3 | ||||
| chr9:33025090-33025378 | Common:7; Rare:121 | ||||
| chr9:33025672-33025827 | Common:3; Rare:71 | ||||
| chr9:33166798-33166883 | Rare:26; Clinvar:2 | ||||
| chr9:33290380-33290581 | Common:2; Rare:77 | ||||
| chr9:33473896-33474140 | Common:1; Rare:61 |