| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101398570-101398887 | Common:1; Rare:110 | ||||
| chr9:101533700-101533925 | Rare:70 | ||||
| chr9:104093977-104094389 | Common:5; Rare:105 | ||||
| chr9:104094509-104094604 | Common:2; Rare:32 | ||||
| chr9:104747535-104747799 | Common:1; Rare:78 | ||||
| chr9:105558067-105558170 | Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:105694406-105694612 | Common:3; Rare:89 | ||||
| chr9:107283051-107283279 | Common:1; Rare:76 | ||||
| chr9:108934074-108934477 | Common:7; Rare:161; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110048374-110048718 | Common:1; Rare:86 | ||||
| chr9:110148502-110148666 | Common:1; Rare:37 | ||||
| chr9:110256431-110256672 | Common:2; Rare:93 | ||||
| chr9:111661484-111661673 | Common:3; Rare:55 | ||||
| chr9:112333565-112333951 | Rare:122 | ||||
| chr9:112379834-112380132 | Common:3; Rare:118 |