| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35604027-35604356 | Common:3; Rare:91 | ||||
| chr9:35728435-35728718 | Common:1; Rare:48 | ||||
| chr9:35914610-35914654 | Rare:7 | ||||
| chr9:35929334-35929493 | Rare:26 | ||||
| chr9:36236866-36237093 | Rare:49; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr9:38437564-38437750 | Common:3; Rare:36 | ||||
| chr9:39464482-39464670 | Common:1; Rare:44 | ||||
| chr9:40991948-40992410 | Common:7; Rare:33 | ||||
| chr9:62801376-62801489 | Common:1; Rare:1 | ||||
| chr9:63326878-63326997 | Rare:6 | ||||
| chr9:63859605-63859741 | Common:3; Rare:12 | ||||
| chr9:66269890-66270057 | Common:1; Rare:30 | ||||
| chr9:68975831-68975883 | Rare:8 | ||||
| chr9:70258254-70258350 | Common:1; Rare:19 | ||||
| chr9:70413394-70413611 | Rare:69 |