| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104747634-104747748 | Rare:25 | ||||
| chr9:108934065-108934484 | Common:7; Rare:166; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110127395-110127479 | Rare:9 | ||||
| chr9:110579188-110579271 | Rare:30 | ||||
| chr9:110580062-110580103 | Rare:5 | ||||
| chr9:112333576-112333944 | Rare:117 | ||||
| chr9:112379800-112380157 | Common:3; Rare:142 | ||||
| chr9:113221247-113221622 | Common:1; Rare:118 | ||||
| chr9:113275396-113275708 | Common:5; Rare:98; Clinvar (pathogenic):1 | ||||
| chr9:113410661-113410810 | Common:2; Rare:57 | ||||
| chr9:116687211-116687334 | Common:3; Rare:39; Clinvar (benign):1 | ||||
| chr9:120477449-120477537 | Rare:18; Clinvar:1 | ||||
| chr9:120793249-120793536 | Common:1; Rare:106 | ||||
| chr9:120842905-120843095 | Common:1; Rare:66 | ||||
| chr9:121074851-121074959 | Rare:54 |