| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37592498-37592673 | Common:2; Rare:62 | ||||
| chr9:37785024-37785132 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:37800696-37800794 | Rare:28 | ||||
| chr9:37904084-37904463 | Common:3; Rare:121 | ||||
| chr9:68779910-68780166 | Common:3; Rare:94 | ||||
| chr9:69759935-69760152 | Common:3; Rare:96 | ||||
| chr9:70258829-70259069 | Common:4; Rare:114 | ||||
| chr9:70413930-70414205 | Rare:56 | ||||
| chr9:70414303-70414517 | Rare:49 | ||||
| chr9:71911173-71911508 | Common:3; Rare:96 | ||||
| chr9:74497123-74497337 | Common:3; Rare:48 | ||||
| chr9:75088140-75088621 | Common:3; Rare:165 | ||||
| chr9:76459015-76459285 | Common:1; Rare:89 | ||||
| chr9:78235990-78236107 | Rare:37 | ||||
| chr9:78296915-78297206 | Common:2; Rare:83; Clinvar (benign):1 |