| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:91361768-91362081 | Common:4; Rare:174; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:91423775-91424063 | Common:2; Rare:174 | ||||
| chr9:92115336-92115512 | Common:2; Rare:107; Clinvar:2 | ||||
| chr9:92293588-92293965 | Common:12; Rare:240 | ||||
| chr9:92325284-92325991 | Common:18; Rare:368 | ||||
| chr9:92670024-92670423 | Common:2; Rare:240 | ||||
| chr9:92764778-92765051 | Common:4; Rare:178; Clinvar (benign):1 | ||||
| chr9:92877933-92878153 | Common:3; Rare:69 | ||||
| chr9:93058301-93058761 | Common:7; Rare:243 | ||||
| chr9:93134139-93134369 | Common:3; Rare:123 | ||||
| chr9:93451473-93451893 | Common:6; Rare:207 | ||||
| chr9:93453528-93453770 | Common:2; Rare:106 | ||||
| chr9:93576470-93576768 | Common:6; Rare:120 | ||||
| chr9:94030697-94030872 | Common:2; Rare:91 | ||||
| chr9:94259270-94259382 | Common:1; Rare:32 |