| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:126557723-126557848 | Rare:32 | ||||
| chr8:127736950-127737131 | Rare:43 | ||||
| chr8:127737520-127737801 | Common:2; Rare:72 | ||||
| chr8:130277192-130277395 | Common:3; Rare:47 | ||||
| chr8:140596963-140597318 | Common:2; Rare:74 | ||||
| chr8:140597866-140597988 | Common:1; Rare:32 | ||||
| chr8:140839207-140839355 | Common:2; Rare:33 | ||||
| chr8:142475575-142475859 | Common:3; Rare:40 | ||||
| chr8:145002887-145003041 | Common:1; Rare:49 | ||||
| chr9:6006890-6007216 | Common:3; Rare:116 | ||||
| chr9:6750997-6751114 | Common:1; Rare:26 | ||||
| chr9:6759017-6759066 | Common:1; Rare:13 | ||||
| chr9:7799258-7799452 | Common:4; Rare:60 | ||||
| chr9:32550860-32551103 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33029993-33030123 | Common:1; Rare:41 |