| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34665373-34665660 | Rare:94 | ||||
| chr9:34666020-34666173 | Common:1; Rare:31 | ||||
| chr9:34989348-34989775 | Common:2; Rare:114 | ||||
| chr9:35072371-35072433 | Rare:19; Clinvar:1 | ||||
| chr9:35079926-35080153 | Common:4; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:35103078-35103297 | Common:1; Rare:78 | ||||
| chr9:35112390-35112503 | Common:2; Rare:22 | ||||
| chr9:35115836-35116146 | Common:1; Rare:56 | ||||
| chr9:35161780-35162084 | Common:4; Rare:88 | ||||
| chr9:35489922-35490127 | Common:1; Rare:56 | ||||
| chr9:35563870-35563990 | Rare:35 | ||||
| chr9:35646776-35646951 | Rare:40 | ||||
| chr9:35657836-35658495 | Common:12; Rare:488; Clinvar:44; Clinvar (benign):17; Clinvar (pathogenic):40 | ||||
| chr9:35673887-35673955 | Common:2; Rare:18 | ||||
| chr9:35685432-35685781 | Common:1; Rare:81; Clinvar (benign):5; Clinvar (pathogenic):2 |