| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:70414006-70414188 | Rare:35 | ||||
| chr9:71911173-71911499 | Common:2; Rare:93 | ||||
| chr9:72149358-72149551 | Common:1; Rare:61 | ||||
| chr9:72365180-72365420 | Common:2; Rare:87 | ||||
| chr9:72952939-72953217 | Common:1; Rare:63 | ||||
| chr9:74952210-74952424 | Rare:68 | ||||
| chr9:74952910-74952995 | Rare:19 | ||||
| chr9:75088093-75088612 | Common:4; Rare:174 | ||||
| chr9:76394287-76394569 | Common:7; Rare:100 | ||||
| chr9:78236005-78236141 | Rare:51 | ||||
| chr9:78296908-78297213 | Common:2; Rare:89; Clinvar (benign):1 | ||||
| chr9:81688339-81688626 | Common:5; Rare:100 | ||||
| chr9:81689446-81689853 | Common:10; Rare:165 | ||||
| chr9:83707677-83708374 | Common:7; Rare:238 | ||||
| chr9:83921405-83921595 | Common:2; Rare:78 |