| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98943446-98943585 | Rare:22 | ||||
| chr9:98943684-98943958 | Common:4; Rare:80 | ||||
| chr9:99221906-99222341 | Common:2; Rare:167; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99821711-99822031 | Rare:82 | ||||
| chr9:99906574-99906711 | Rare:66 | ||||
| chr9:100098964-100099314 | Common:3; Rare:99; Clinvar:2 | ||||
| chr9:100352844-100353081 | Rare:86 | ||||
| chr9:101398502-101398910 | Common:1; Rare:145 | ||||
| chr9:101486790-101487195 | Common:2; Rare:88 | ||||
| chr9:104093985-104094321 | Common:3; Rare:78 | ||||
| chr9:104747611-104747832 | Common:1; Rare:75 | ||||
| chr9:104764021-104764207 | Common:2; Rare:45 | ||||
| chr9:105558046-105558163 | Rare:38; Clinvar (benign):1 | ||||
| chr9:106863009-106863180 | Rare:60 | ||||
| chr9:106863527-106863630 | Rare:20 |