| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100447834-100447966 | Rare:17 | ||||
| chr9:100449345-100449586 | Common:1; Rare:37 | ||||
| chr9:100455828-100456029 | Rare:31 | ||||
| chr9:101540240-101540559 | Common:1; Rare:85 | ||||
| chr9:101540561-101540806 | Common:1; Rare:59 | ||||
| chr9:101546862-101547171 | Common:1; Rare:75 | ||||
| chr9:104100100-104100430 | Common:3; Rare:76 | ||||
| chr9:105537811-105538086 | Common:2; Rare:42 | ||||
| chr9:108874893-108874895 | |||||
| chr9:108918677-108918819 | Rare:27 | ||||
| chr9:108919290-108919607 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:108940808-108941112 | Rare:52 | ||||
| chr9:108942493-108942645 | Rare:31 | ||||
| chr9:108943007-108943135 | Common:1; Rare:33 | ||||
| chr9:108943715-108944021 | Rare:81 |