| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:18508967-18509386 | Common:2; Rare:84 | ||||
| chr7:22822775-22822963 | Common:3; Rare:71 | ||||
| chr7:23105673-23105829 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181864-23182083 | Common:1; Rare:90 | ||||
| chr7:23470345-23470560 | Rare:66 | ||||
| chr7:23531966-23532098 | Rare:52 | ||||
| chr7:25125245-25125608 | Rare:145; Clinvar:3 | ||||
| chr7:26201417-26201805 | Common:2; Rare:185 | ||||
| chr7:27095965-27096229 | Rare:75 | ||||
| chr7:27740102-27740212 | Common:3; Rare:32 | ||||
| chr7:30504775-30505076 | Common:2; Rare:95 | ||||
| chr7:30594733-30594949 | Common:3; Rare:102; Clinvar:5; Clinvar (benign):6 | ||||
| chr7:32495258-32495564 | Rare:75 | ||||
| chr7:33062714-33062923 | Common:3; Rare:90 | ||||
| chr7:35800988-35801258 | Common:1; Rare:117 |