| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100427034-100427390 | Common:7; Rare:129 | ||||
| chr9:101398503-101398912 | Common:1; Rare:146 | ||||
| chr9:101487043-101487221 | Common:2; Rare:49 | ||||
| chr9:101533703-101533914 | Rare:64 | ||||
| chr9:104093979-104094347 | Common:3; Rare:90 | ||||
| chr9:104094431-104094614 | Common:2; Rare:50 | ||||
| chr9:104747535-104747808 | Common:1; Rare:81 | ||||
| chr9:104747840-104747961 | Common:3; Rare:42 | ||||
| chr9:104928131-104928466 | Common:6; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:105244505-105244855 | Common:3; Rare:123 | ||||
| chr9:105245095-105245141 | Rare:14 | ||||
| chr9:105447924-105448144 | Common:4; Rare:79 | ||||
| chr9:105558044-105558175 | Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:105694409-105694663 | Common:3; Rare:117 | ||||
| chr9:106862365-106862676 | Common:4; Rare:88 |