| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34049339-34049588 | Common:1; Rare:75 | ||||
| chr9:34125680-34125804 | Rare:24 | ||||
| chr9:34126347-34126824 | Common:1; Rare:160 | ||||
| chr9:34178928-34179163 | Common:1; Rare:58 | ||||
| chr9:34179250-34179436 | Rare:32 | ||||
| chr9:34329181-34329640 | Common:1; Rare:143 | ||||
| chr9:34381519-34381847 | Rare:51 | ||||
| chr9:34397752-34397881 | Common:1; Rare:15 | ||||
| chr9:34458555-34459088 | Common:2; Rare:134; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:34491371-34491549 | Rare:45; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:34612037-34612223 | Common:9; Rare:68 | ||||
| chr9:34616085-34616154 | Rare:12 | ||||
| chr9:34620440-34620645 | Common:1; Rare:55 | ||||
| chr9:34637720-34638153 | Common:3; Rare:111 | ||||
| chr9:34652001-34652217 | Rare:64 |