| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113275392-113275699 | Common:5; Rare:93; Clinvar (pathogenic):1 | ||||
| chr9:116153565-116153835 | Common:1; Rare:62 | ||||
| chr9:116687244-116687376 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:120793369-120793475 | Rare:41 | ||||
| chr9:120842912-120843095 | Common:1; Rare:64 | ||||
| chr9:121201858-121202112 | Common:2; Rare:68 | ||||
| chr9:121370203-121370516 | Common:2; Rare:93 | ||||
| chr9:122264786-122264915 | Common:2; Rare:40 | ||||
| chr9:124861893-124862125 | Rare:99 | ||||
| chr9:125189728-125190029 | Common:1; Rare:140 | ||||
| chr9:127451369-127451523 | Common:1; Rare:55 | ||||
| chr9:127578998-127579221 | Common:3; Rare:38 | ||||
| chr9:128191512-128191723 | Common:1; Rare:58 | ||||
| chr9:128275914-128276293 | Common:4; Rare:167 | ||||
| chr9:128683525-128683836 | Rare:58 |