| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99500200-99500472 | Common:6; Rare:114 | ||||
| chr7:99504460-99504730 | Common:1; Rare:110 | ||||
| chr7:99504750-99505130 | Rare:129 | ||||
| chr7:99552080-99552215 | Rare:62 | ||||
| chr7:99558483-99558902 | Common:7; Rare:222 | ||||
| chr7:99616400-99616670 | Common:2; Rare:122 | ||||
| chr7:99616807-99617019 | Common:4; Rare:128 | ||||
| chr7:99919375-99919697 | Rare:199 | ||||
| chr7:100015508-100015664 | Common:2; Rare:81 | ||||
| chr7:100049717-100049842 | Rare:52 | ||||
| chr7:100081663-100081998 | Common:5; Rare:178 | ||||
| chr7:100088864-100089068 | Common:2; Rare:135 | ||||
| chr7:100100719-100100904 | Common:4; Rare:136 | ||||
| chr7:100101316-100101717 | Common:2; Rare:299; Clinvar (benign):1 | ||||
| chr7:100119225-100119728 | Common:1; Rare:282 |