| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:98304383-98304547 | Common:2; Rare:47 | ||||
| chr7:98315459-98315764 | Common:9; Rare:91; Clinvar (benign):1 | ||||
| chr7:98320240-98320405 | Common:2; Rare:45 | ||||
| chr7:98322905-98322984 | Rare:9 | ||||
| chr7:98335923-98336142 | Common:1; Rare:38 | ||||
| chr7:99022941-99023058 | Common:2; Rare:18 | ||||
| chr7:99023327-99023420 | Rare:12 | ||||
| chr7:99038254-99038282 | Rare:4 | ||||
| chr7:99038380-99038713 | Rare:110 | ||||
| chr7:99040457-99040638 | Rare:50 | ||||
| chr7:99042149-99042474 | Rare:69 | ||||
| chr7:99045992-99046280 | Common:2; Rare:45 | ||||
| chr7:99051389-99051638 | Rare:52 | ||||
| chr7:99060679-99060983 | Common:2; Rare:60 | ||||
| chr7:99061796-99062098 | Common:1; Rare:59 |