| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26201192-26201555 | Rare:143 | ||||
| chr7:26201577-26201805 | Common:2; Rare:122 | ||||
| chr7:27096011-27096261 | Rare:67 | ||||
| chr7:27102966-27103236 | Common:1; Rare:57 | ||||
| chr7:27740083-27740218 | Common:3; Rare:40 | ||||
| chr7:28180547-28180860 | Common:4; Rare:87 | ||||
| chr7:28958289-28958530 | Rare:69 | ||||
| chr7:30284348-30284745 | Common:6; Rare:162 | ||||
| chr7:30478681-30478977 | Common:6; Rare:102; Clinvar:1 | ||||
| chr7:30504758-30505079 | Common:2; Rare:106 | ||||
| chr7:30594722-30594975 | Common:3; Rare:123; Clinvar:6; Clinvar (benign):7 | ||||
| chr7:30771304-30771494 | Common:1; Rare:66 | ||||
| chr7:30911643-30912129 | Common:2; Rare:152; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:32070785-32071113 | Common:3; Rare:79 | ||||
| chr7:32495240-32495621 | Common:1; Rare:97 |