| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:110256410-110256720 | Common:4; Rare:108 | ||||
| chr9:110579296-110579423 | Rare:43 | ||||
| chr9:110579869-110580097 | Common:1; Rare:52 | ||||
| chr9:111599785-111600136 | Common:4; Rare:86 | ||||
| chr9:111631177-111631317 | Rare:24 | ||||
| chr9:111661487-111661703 | Common:3; Rare:61 | ||||
| chr9:111897028-111897188 | Common:2; Rare:51 | ||||
| chr9:112379770-112380187 | Common:4; Rare:156 | ||||
| chr9:113056674-113056848 | Rare:63 | ||||
| chr9:113150862-113151040 | Common:1; Rare:60 | ||||
| chr9:113188022-113188186 | Common:2; Rare:19 | ||||
| chr9:113221235-113221617 | Common:1; Rare:121 | ||||
| chr9:113275380-113275734 | Common:5; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:113376914-113377127 | Common:8; Rare:70 | ||||
| chr9:113410289-113410729 | Common:3; Rare:133 |