| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74657459-74657788 | Common:2; Rare:91 | ||||
| chr7:74657944-74658067 | Common:1; Rare:27 | ||||
| chr7:75878805-75879179 | Common:12; Rare:132 | ||||
| chr7:75914898-75915236 | Common:4; Rare:122; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75994488-75994791 | Common:4; Rare:149 | ||||
| chr7:76047946-76048220 | Common:2; Rare:97 | ||||
| chr7:76302511-76302735 | Common:3; Rare:86; Clinvar:5; Clinvar (benign):4 | ||||
| chr7:76302820-76303075 | Rare:111; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr7:76303565-76303865 | Common:1; Rare:129; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:76439609-76439714 | Common:1; Rare:8 | ||||
| chr7:76627251-76627380 | Common:5; Rare:36 | ||||
| chr7:77122285-77122671 | Common:2; Rare:77 | ||||
| chr7:77416309-77416605 | Common:4; Rare:78 | ||||
| chr7:77537398-77537545 | Rare:51 | ||||
| chr7:77537976-77538073 | Common:3; Rare:46 |