| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906601-99906711 | Rare:51 | ||||
| chr9:100098964-100099314 | Common:3; Rare:99; Clinvar:2 | ||||
| chr9:100352831-100353050 | Rare:71 | ||||
| chr9:101398580-101398895 | Common:1; Rare:107 | ||||
| chr9:101533664-101533914 | Common:2; Rare:79 | ||||
| chr9:104093985-104094321 | Common:3; Rare:78 | ||||
| chr9:104094431-104094638 | Common:3; Rare:59 | ||||
| chr9:104747608-104747779 | Rare:51 | ||||
| chr9:105558086-105558159 | Rare:19; Clinvar (benign):1 | ||||
| chr9:107282967-107283284 | Common:2; Rare:109 | ||||
| chr9:108933951-108933991 | Common:1; Rare:17; Clinvar:4 | ||||
| chr9:108934055-108934487 | Common:7; Rare:172; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110256416-110256665 | Common:2; Rare:95 | ||||
| chr9:110580062-110580160 | Rare:19 | ||||
| chr9:111038181-111038368 | Common:2; Rare:55 |