| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101398594-101398917 | Common:1; Rare:103 | ||||
| chr9:111631201-111631369 | Common:1; Rare:51 | ||||
| chr9:112379811-112380135 | Common:3; Rare:130 | ||||
| chr9:113221262-113221598 | Rare:106 | ||||
| chr9:113275489-113275728 | Common:2; Rare:91; Clinvar (pathogenic):1 | ||||
| chr9:120793369-120793475 | Rare:41 | ||||
| chr9:120842920-120843084 | Common:1; Rare:52 | ||||
| chr9:121201858-121202141 | Common:2; Rare:78 | ||||
| chr9:121370203-121370538 | Common:2; Rare:96 | ||||
| chr9:122264779-122264916 | Common:2; Rare:43 | ||||
| chr9:123268564-123268694 | Common:1; Rare:40 | ||||
| chr9:124861865-124862128 | Common:1; Rare:115 | ||||
| chr9:125200418-125200589 | Common:1; Rare:67 | ||||
| chr9:127451366-127451523 | Common:2; Rare:56 | ||||
| chr9:127877667-127877775 | Rare:22 |