| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:93232259-93232396 | Common:2; Rare:25 | ||||
| chr7:94425753-94426038 | Rare:90; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:94656100-94656447 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:94908385-94908445 | Rare:7 | ||||
| chr7:95596512-95596699 | Common:2; Rare:37 | ||||
| chr7:96709759-96709891 | Rare:51 | ||||
| chr7:97024822-97025114 | Common:2; Rare:63 | ||||
| chr7:97117448-97117759 | Common:2; Rare:132 | ||||
| chr7:98252143-98252372 | Common:1; Rare:54 | ||||
| chr7:98869934-98870098 | Rare:55 | ||||
| chr7:99325784-99325963 | Common:1; Rare:71 | ||||
| chr7:99408555-99408706 | Common:2; Rare:44 | ||||
| chr7:99408710-99409063 | Common:1; Rare:99 | ||||
| chr7:99438721-99438977 | Common:1; Rare:81 | ||||
| chr7:99460108-99460304 | Rare:63 |