| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34653754-34653978 | Rare:42 | ||||
| chr9:34665368-34665660 | Rare:96 | ||||
| chr9:34665977-34666219 | Common:3; Rare:65 | ||||
| chr9:34989406-34989790 | Common:2; Rare:98 | ||||
| chr9:35079648-35079839 | Rare:34 | ||||
| chr9:35079908-35080190 | Common:5; Rare:77; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:35096560-35096622 | Rare:12 | ||||
| chr9:35103049-35103295 | Common:1; Rare:91 | ||||
| chr9:35161819-35162141 | Common:4; Rare:92 | ||||
| chr9:35489922-35490142 | Common:3; Rare:62 | ||||
| chr9:35538711-35538912 | Common:1; Rare:43 | ||||
| chr9:35657855-35658376 | Common:8; Rare:435; Clinvar:42; Clinvar (benign):15; Clinvar (pathogenic):40 | ||||
| chr9:35665165-35665353 | Common:2; Rare:73 | ||||
| chr9:35689798-35690123 | Common:4; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35691066-35691225 | Common:1; Rare:34 |