| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133273782-133273963 | Common:1; Rare:31 | ||||
| chr9:133274402-133274633 | Common:1; Rare:47 | ||||
| chr9:133275913-133276052 | Common:1; Rare:34 | ||||
| chr9:133334195-133334396 | Common:1; Rare:54 | ||||
| chr9:133349553-133350052 | Common:1; Rare:186 | ||||
| chr9:133937883-133938194 | Common:3; Rare:65 | ||||
| chr9:134335970-134336149 | Rare:44 | ||||
| chr9:134811332-134811590 | Rare:81; Clinvar:7; Clinvar (benign):5 | ||||
| chr9:136400162-136400271 | Common:1; Rare:34 | ||||
| chr9:136673921-136673932 | Rare:4; Clinvar (pathogenic):1 | ||||
| chr9:136674718-136674876 | Common:1; Rare:52; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr9:136693690-136694005 | Common:1; Rare:53 | ||||
| chr9:136803088-136803134 | |||||
| chr9:136803223-136803500 | Common:8; Rare:77 | ||||
| chr9:136838605-136839030 | Common:6; Rare:158 |