| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34652010-34652214 | Rare:58 | ||||
| chr9:34665373-34665655 | Rare:92 | ||||
| chr9:35103100-35103297 | Common:1; Rare:62 | ||||
| chr9:35161848-35162151 | Common:4; Rare:88 | ||||
| chr9:35489881-35490139 | Common:2; Rare:76 | ||||
| chr9:35657841-35658376 | Common:9; Rare:443; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35689702-35689775 | Rare:19; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35689777-35690123 | Common:4; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35732073-35732334 | Common:2; Rare:70 | ||||
| chr9:35732373-35732676 | Common:2; Rare:76 | ||||
| chr9:35748989-35749351 | Common:2; Rare:135 | ||||
| chr9:35814983-35815235 | Rare:70 | ||||
| chr9:36190703-36190994 | Common:1; Rare:100 | ||||
| chr9:36258395-36258607 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37576238-37576403 | Rare:47 |