| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73557074-73557392 | Common:2; Rare:112 | ||||
| chr7:73683175-73683201 | Rare:11 | ||||
| chr7:73683399-73683794 | Common:4; Rare:173 | ||||
| chr7:73738786-73739024 | Common:1; Rare:69 | ||||
| chr7:74028046-74028261 | Common:1; Rare:80; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:74045091-74045286 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:74254352-74254535 | Rare:85 | ||||
| chr7:74657493-74657794 | Common:2; Rare:84 | ||||
| chr7:75914944-75915164 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994498-75994772 | Common:4; Rare:135 | ||||
| chr7:76047950-76048200 | Common:2; Rare:86 | ||||
| chr7:76302520-76303076 | Common:3; Rare:233; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303745-76303865 | Rare:60; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:77122265-77122672 | Common:2; Rare:84 | ||||
| chr7:77199168-77199452 | Rare:91 |