| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:120868818-120869137 | Common:2; Rare:75 | ||||
| chr9:120877157-120877482 | Common:3; Rare:107 | ||||
| chr9:120929114-120929183 | Common:1; Rare:15 | ||||
| chr9:121074849-121074977 | Rare:62 | ||||
| chr9:121075109-121075332 | Rare:52 | ||||
| chr9:121201787-121202149 | Common:2; Rare:114 | ||||
| chr9:121268053-121268225 | Common:1; Rare:57 | ||||
| chr9:121281673-121281894 | Rare:60 | ||||
| chr9:121286048-121286146 | Rare:26 | ||||
| chr9:121299637-121300012 | Common:3; Rare:120; Clinvar:3 | ||||
| chr9:121328886-121329315 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:121370145-121370516 | Common:2; Rare:109 | ||||
| chr9:121566868-121567182 | Rare:82 | ||||
| chr9:122159668-122159939 | Rare:114 | ||||
| chr9:122264603-122264691 | Common:1; Rare:15 |