| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73683399-73683659 | Common:3; Rare:118 | ||||
| chr7:73738786-73738991 | Common:1; Rare:60 | ||||
| chr7:74254373-74254520 | Rare:66 | ||||
| chr7:75914944-75915189 | Common:2; Rare:89; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75994498-75994791 | Common:4; Rare:145 | ||||
| chr7:76047864-76048220 | Common:3; Rare:121 | ||||
| chr7:76302468-76302759 | Common:3; Rare:113; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr7:76302810-76303073 | Rare:115; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr7:77696253-77696493 | Rare:104 | ||||
| chr7:77798387-77798971 | Common:1; Rare:139 | ||||
| chr7:79452909-79452989 | Common:1; Rare:18 | ||||
| chr7:79453556-79453698 | Rare:36 | ||||
| chr7:79453909-79454117 | Common:1; Rare:51 | ||||
| chr7:82443584-82443885 | Common:2; Rare:97 | ||||
| chr7:87152314-87152480 | Common:1; Rare:55 |