| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:132971009-132971578 | Common:3; Rare:91 | ||||
| chr8:132971702-132971912 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:132972483-132973212 | Common:10; Rare:160; Clinvar:1 | ||||
| chr8:133017472-133017626 | Rare:29 | ||||
| chr8:133017676-133018287 | Common:5; Rare:165; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr8:133039828-133040795 | Common:14; Rare:223 | ||||
| chr8:133060604-133060787 | Rare:35 | ||||
| chr8:133074820-133075469 | Common:9; Rare:118 | ||||
| chr8:133075471-133075662 | Common:4; Rare:43 | ||||
| chr8:133094912-133094950 | Rare:4 | ||||
| chr8:133094965-133095271 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:133113370-133114075 | Common:6; Rare:174; Clinvar:6; Clinvar (benign):2 | ||||
| chr8:133133437-133133960 | Common:4; Rare:134 | ||||
| chr8:133190761-133191039 | Common:1; Rare:55 | ||||
| chr8:133297118-133297500 | Common:3; Rare:144; Clinvar:4; Clinvar (benign):2 |