| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113275359-113275689 | Common:4; Rare:91; Clinvar (pathogenic):1 | ||||
| chr9:113340295-113340430 | Common:1; Rare:30 | ||||
| chr9:113410281-113410729 | Common:3; Rare:135 | ||||
| chr9:114587565-114587856 | Common:3; Rare:116 | ||||
| chr9:116687220-116687361 | Common:3; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793353-120793538 | Common:2; Rare:77 | ||||
| chr9:120842905-120843045 | Common:1; Rare:46 | ||||
| chr9:120877186-120877512 | Common:1; Rare:113 | ||||
| chr9:121074849-121074993 | Rare:75 | ||||
| chr9:121201838-121202149 | Common:2; Rare:89 | ||||
| chr9:121268041-121268198 | Common:1; Rare:57 | ||||
| chr9:121370175-121370458 | Common:2; Rare:82 | ||||
| chr9:122159723-122159911 | Rare:64 | ||||
| chr9:122264810-122264917 | Common:1; Rare:30 | ||||
| chr9:122905281-122905598 | Common:2; Rare:115 |