| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104094522-104094614 | Common:1; Rare:30 | ||||
| chr9:108934100-108934487 | Common:7; Rare:158; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:112379834-112380150 | Common:3; Rare:130 | ||||
| chr9:113221262-113221597 | Rare:106 | ||||
| chr9:113275354-113275728 | Common:5; Rare:121; Clinvar (pathogenic):1 | ||||
| chr9:113410394-113410756 | Common:3; Rare:103 | ||||
| chr9:120793341-120793534 | Common:1; Rare:82 | ||||
| chr9:120842917-120843239 | Common:1; Rare:101 | ||||
| chr9:120877125-120877532 | Common:3; Rare:134 | ||||
| chr9:121074851-121074977 | Rare:61 | ||||
| chr9:121201839-121202149 | Common:2; Rare:89 | ||||
| chr9:122264737-122264922 | Common:2; Rare:53 | ||||
| chr9:122905281-122905509 | Common:1; Rare:99 | ||||
| chr9:124861908-124862116 | Rare:90 | ||||
| chr9:124940975-124941168 | Common:3; Rare:64 |