| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35673859-35673938 | Common:2; Rare:22 | ||||
| chr9:35689146-35689435 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:35732074-35732334 | Common:2; Rare:70 | ||||
| chr9:35732373-35732683 | Common:3; Rare:78 | ||||
| chr9:35748946-35749369 | Common:2; Rare:151 | ||||
| chr9:35814975-35815262 | Rare:74 | ||||
| chr9:35829120-35829280 | Common:1; Rare:44 | ||||
| chr9:36190757-36191003 | Rare:80 | ||||
| chr9:36258386-36258643 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37422631-37422735 | Common:2; Rare:59 | ||||
| chr9:37485737-37486002 | Common:1; Rare:94 | ||||
| chr9:37800707-37800816 | Rare:30 | ||||
| chr9:37904076-37904463 | Common:3; Rare:127 | ||||
| chr9:38392569-38392777 | Common:2; Rare:60 | ||||
| chr9:66900587-66900804 | Common:3; Rare:68 |