| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73827911-73828227 | Common:5; Rare:78 | ||||
| chr7:73842506-73842693 | Common:6; Rare:27 | ||||
| chr7:74083885-74084040 | Rare:34 | ||||
| chr7:74174088-74174412 | Common:1; Rare:158 | ||||
| chr7:74174482-74174704 | Common:2; Rare:65 | ||||
| chr7:74254315-74254535 | Rare:103 | ||||
| chr7:74289203-74289479 | Common:4; Rare:95 | ||||
| chr7:74454056-74454157 | Rare:28 | ||||
| chr7:74657473-74657985 | Common:3; Rare:140 | ||||
| chr7:74658474-74658781 | Common:1; Rare:82 | ||||
| chr7:75073464-75073615 | Rare:45 | ||||
| chr7:75073724-75073892 | Common:2; Rare:59 | ||||
| chr7:75878826-75879111 | Common:12; Rare:105 | ||||
| chr7:75914905-75915175 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994489-75994792 | Common:5; Rare:149 |