| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94423413-94423520 | Rare:21 | ||||
| chr7:94425746-94426297 | Common:1; Rare:132; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:94656036-94656376 | Common:2; Rare:93; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:95434935-95435143 | Common:1; Rare:102; Clinvar (benign):1 | ||||
| chr7:97872360-97872593 | Common:2; Rare:77 | ||||
| chr7:98252133-98252372 | Common:1; Rare:54 | ||||
| chr7:98281608-98281746 | Common:3; Rare:53 | ||||
| chr7:99143818-99143877 | Rare:22 | ||||
| chr7:99325781-99325997 | Common:1; Rare:87 | ||||
| chr7:99408537-99408665 | Common:2; Rare:43 | ||||
| chr7:99408667-99409114 | Common:1; Rare:118 | ||||
| chr7:99438728-99439005 | Common:1; Rare:86 | ||||
| chr7:99439273-99439479 | Common:2; Rare:49 | ||||
| chr7:99466131-99466270 | Rare:49 | ||||
| chr7:99500238-99500417 | Common:2; Rare:50 |