| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35814980-35815275 | Rare:74 | ||||
| chr9:36190725-36190994 | Common:1; Rare:88 | ||||
| chr9:36258404-36258580 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37120183-37120536 | Common:2; Rare:101 | ||||
| chr9:37800702-37800816 | Rare:30 | ||||
| chr9:37904076-37904203 | Rare:41 | ||||
| chr9:68356354-68356628 | Common:7; Rare:47 | ||||
| chr9:68779960-68780152 | Common:2; Rare:63 | ||||
| chr9:69173883-69174250 | Common:6; Rare:114 | ||||
| chr9:70258772-70259069 | Common:4; Rare:129 | ||||
| chr9:70414078-70414203 | Rare:29 | ||||
| chr9:70414299-70414358 | Rare:11 | ||||
| chr9:70414370-70414403 | Rare:6 | ||||
| chr9:71911184-71911668 | Common:3; Rare:134 | ||||
| chr9:72364513-72364920 | Common:4; Rare:137 |