| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112379834-112380150 | Common:3; Rare:130 | ||||
| chr9:113150644-113151022 | Common:5; Rare:85 | ||||
| chr9:113221230-113221615 | Common:1; Rare:122 | ||||
| chr9:113275359-113275728 | Common:5; Rare:118; Clinvar (pathogenic):1 | ||||
| chr9:113410290-113410729 | Common:3; Rare:132 | ||||
| chr9:116687203-116687361 | Common:3; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793256-120793533 | Common:1; Rare:101 | ||||
| chr9:120842908-120843089 | Common:1; Rare:65 | ||||
| chr9:120868827-120869113 | Common:2; Rare:61 | ||||
| chr9:121074858-121074967 | Rare:52 | ||||
| chr9:121201846-121202149 | Common:2; Rare:85 | ||||
| chr9:122159723-122159936 | Rare:74 | ||||
| chr9:122264381-122264617 | Common:2; Rare:48 | ||||
| chr9:122264737-122264922 | Common:2; Rare:53 | ||||
| chr9:122905257-122905592 | Common:2; Rare:120 |