| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34329187-34329593 | Rare:129 | ||||
| chr9:34458539-34458896 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:34612084-34612223 | Common:8; Rare:46 | ||||
| chr9:34652032-34652201 | Rare:47 | ||||
| chr9:34665379-34665660 | Rare:91 | ||||
| chr9:35161782-35162061 | Common:4; Rare:79 | ||||
| chr9:35646823-35646962 | Common:1; Rare:27 | ||||
| chr9:35657855-35657884 | Common:1; Rare:25; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr9:35657899-35658326 | Common:5; Rare:364; Clinvar:32; Clinvar (benign):13; Clinvar (pathogenic):37 | ||||
| chr9:35689807-35690120 | Common:4; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35732083-35732334 | Common:2; Rare:70 | ||||
| chr9:35732400-35732683 | Common:3; Rare:68 | ||||
| chr9:35748999-35749342 | Common:2; Rare:129 | ||||
| chr9:35814983-35815296 | Rare:79 | ||||
| chr9:36258374-36258580 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 |