| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35731964-35732334 | Common:2; Rare:93 | ||||
| chr9:35732365-35732877 | Common:4; Rare:128 | ||||
| chr9:35737844-35738190 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:35748545-35748770 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:35748859-35749408 | Common:4; Rare:180 | ||||
| chr9:35749648-35749776 | Rare:43 | ||||
| chr9:35814983-35815294 | Rare:79 | ||||
| chr9:35905942-35906302 | Common:1; Rare:91 | ||||
| chr9:36190703-36191063 | Common:2; Rare:116 | ||||
| chr9:36258409-36258625 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36276945-36277297 | Common:3; Rare:78; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:36400306-36400579 | Common:1; Rare:80 | ||||
| chr9:36572832-36572949 | Rare:34 | ||||
| chr9:37576274-37576381 | Rare:31 | ||||
| chr9:37800707-37800822 | Rare:34 |