| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98943682-98943958 | Common:4; Rare:82 | ||||
| chr9:99221915-99222365 | Common:2; Rare:178; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:99821670-99821988 | Rare:94 | ||||
| chr9:99906574-99906717 | Rare:67 | ||||
| chr9:100098951-100099342 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352831-100353100 | Rare:98 | ||||
| chr9:101398520-101398910 | Common:1; Rare:140 | ||||
| chr9:101533715-101533905 | Rare:60 | ||||
| chr9:104093985-104094350 | Common:3; Rare:89 | ||||
| chr9:104094431-104094604 | Common:2; Rare:47 | ||||
| chr9:104747608-104747785 | Common:1; Rare:54 | ||||
| chr9:105447976-105448153 | Common:2; Rare:65 | ||||
| chr9:105558033-105558170 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862971-106863189 | Rare:75 | ||||
| chr9:108933957-108934001 | Common:1; Rare:18; Clinvar:4 |