| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74657459-74657722 | Common:2; Rare:79 | ||||
| chr7:74657944-74658067 | Common:1; Rare:27 | ||||
| chr7:75611764-75611991 | Common:1; Rare:45 | ||||
| chr7:75878805-75879094 | Common:12; Rare:104 | ||||
| chr7:75914908-75915213 | Common:4; Rare:111; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75980182-75980488 | Common:2; Rare:93; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:75983524-75983852 | Common:1; Rare:127; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:75985920-75986241 | Common:4; Rare:134; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr7:75994493-75994772 | Common:4; Rare:137 | ||||
| chr7:76047855-76048226 | Common:3; Rare:125 | ||||
| chr7:76302820-76303073 | Rare:111; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr7:77199789-77199891 | Rare:25 | ||||
| chr7:77696122-77696484 | Common:1; Rare:135 | ||||
| chr7:77798355-77798971 | Common:1; Rare:146 | ||||
| chr7:79453548-79453649 | Rare:27 |