| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90346573-90346733 | Common:3; Rare:69 | ||||
| chr7:90595833-90596048 | Common:6; Rare:77 | ||||
| chr7:90596222-90596587 | Common:1; Rare:118 | ||||
| chr7:91880668-91880812 | Common:1; Rare:40 | ||||
| chr7:92134431-92134570 | Rare:42 | ||||
| chr7:92134731-92134891 | Common:3; Rare:47 | ||||
| chr7:92245865-92245970 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528370-92528826 | Common:4; Rare:141; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833906-92834039 | Rare:33 | ||||
| chr7:93232318-93232389 | Common:1; Rare:16 | ||||
| chr7:94656100-94656367 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95396363-95396476 | Common:2; Rare:45 | ||||
| chr7:95434884-95435077 | Common:1; Rare:83; Clinvar (benign):1 | ||||
| chr7:95596162-95596713 | Common:6; Rare:142 | ||||
| chr7:95596877-95596899 | Rare:1 |