| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:686464-686809 | Common:4; Rare:87 | ||||
| chr9:738045-738429 | Common:4; Rare:155; Clinvar:1 | ||||
| chr9:738448-738714 | Common:3; Rare:86 | ||||
| chr9:5768736-5769009 | Common:2; Rare:86 | ||||
| chr9:15468961-15469185 | Common:2; Rare:63 | ||||
| chr9:15469943-15470245 | Rare:89 | ||||
| chr9:15479619-15479772 | Common:1; Rare:51 | ||||
| chr9:15486872-15487047 | Common:1; Rare:56 | ||||
| chr9:16726834-16726933 | Common:1; Rare:21 | ||||
| chr9:25677461-25677675 | Common:3; Rare:93 | ||||
| chr9:32430235-32430559 | Rare:82 | ||||
| chr9:32550829-32551225 | Common:1; Rare:151; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:35604026-35604348 | Common:3; Rare:90 | ||||
| chr9:35684247-35684561 | Rare:71; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:35706766-35707156 | Common:2; Rare:113 |