| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120842863-120843095 | Common:1; Rare:86 | ||||
| chr9:120868827-120869074 | Common:2; Rare:53 | ||||
| chr9:120877186-120877493 | Common:1; Rare:102 | ||||
| chr9:120929123-120929346 | Common:4; Rare:45 | ||||
| chr9:121074756-121075006 | Rare:118 | ||||
| chr9:121075109-121075349 | Rare:55 | ||||
| chr9:121121678-121121829 | Rare:39 | ||||
| chr9:121201805-121202168 | Common:2; Rare:110 | ||||
| chr9:121222964-121223134 | Common:2; Rare:56 | ||||
| chr9:121268064-121268198 | Common:1; Rare:47 | ||||
| chr9:121281615-121281916 | Rare:82 | ||||
| chr9:121327076-121327470 | Common:6; Rare:111; Clinvar (benign):2 | ||||
| chr9:121369809-121369922 | Rare:22 | ||||
| chr9:121370172-121370550 | Common:2; Rare:109 | ||||
| chr9:122093309-122093465 | Common:1; Rare:64 |