| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113565393-113565517 | Common:1; Rare:26 | ||||
| chr9:114587537-114587856 | Common:3; Rare:129 | ||||
| chr9:116687228-116687361 | Common:1; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120580132-120580315 | Rare:55; Clinvar:3 | ||||
| chr9:120793231-120793543 | Common:2; Rare:114 | ||||
| chr9:120842904-120843111 | Common:1; Rare:74 | ||||
| chr9:121074851-121074983 | Rare:66 | ||||
| chr9:121201829-121202172 | Common:2; Rare:99 | ||||
| chr9:121268000-121268207 | Common:1; Rare:68 | ||||
| chr9:121370192-121370512 | Common:2; Rare:98 | ||||
| chr9:122159708-122159904 | Rare:76 | ||||
| chr9:122264721-122264922 | Common:2; Rare:56 | ||||
| chr9:122375197-122375307 | Common:2; Rare:36 | ||||
| chr9:122828500-122828770 | Rare:80 | ||||
| chr9:122905233-122905547 | Common:2; Rare:121 |