| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98056425-98056795 | Common:6; Rare:115 | ||||
| chr9:98255738-98255835 | Rare:31 | ||||
| chr9:99221906-99222365 | Common:2; Rare:182; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:99906588-99906717 | Rare:56 | ||||
| chr9:100098946-100099329 | Common:3; Rare:108; Clinvar:2 | ||||
| chr9:100352831-100353103 | Rare:100 | ||||
| chr9:100429401-100429614 | Rare:35 | ||||
| chr9:101398575-101398887 | Common:1; Rare:107 | ||||
| chr9:101487043-101487221 | Common:2; Rare:49 | ||||
| chr9:101533700-101533907 | Rare:64 | ||||
| chr9:104747535-104747802 | Common:1; Rare:80 | ||||
| chr9:105558067-105558170 | Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:108934074-108934508 | Common:7; Rare:178; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110048498-110048796 | Common:3; Rare:102; Clinvar (benign):1 | ||||
| chr9:112379811-112380154 | Common:3; Rare:138 |