| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121326183-121326421 | Rare:42 | ||||
| chr9:121326614-121326774 | Common:2; Rare:56; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:121328770-121328919 | Common:2; Rare:45; Clinvar (benign):1 | ||||
| chr9:121328927-121329308 | Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:121370183-121370434 | Common:2; Rare:73 | ||||
| chr9:122264600-122264663 | Rare:8 | ||||
| chr9:122264762-122264922 | Common:2; Rare:48 | ||||
| chr9:122913285-122913624 | Common:2; Rare:77 | ||||
| chr9:122931482-122931694 | Common:3; Rare:44 | ||||
| chr9:122940779-122941072 | Common:2; Rare:120 | ||||
| chr9:124861903-124862153 | Common:1; Rare:109 | ||||
| chr9:124940969-124941168 | Common:3; Rare:67 | ||||
| chr9:125189680-125189727 | Rare:14 | ||||
| chr9:125189733-125190019 | Common:1; Rare:133 | ||||
| chr9:125200448-125200590 | Rare:54 |