| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24980107-24980377 | Common:6; Rare:111 | ||||
| chr7:25125205-25125684 | Rare:192; Clinvar:3 | ||||
| chr7:26196397-26196665 | Common:2; Rare:97; Clinvar (benign):3 | ||||
| chr7:26200558-26201277 | Common:3; Rare:329 | ||||
| chr7:26201361-26201818 | Common:2; Rare:213 | ||||
| chr7:26202078-26202430 | Rare:156 | ||||
| chr7:26864551-26864844 | Common:3; Rare:90 | ||||
| chr7:27662794-27663155 | Common:6; Rare:127 | ||||
| chr7:27740022-27740199 | Common:5; Rare:56 | ||||
| chr7:29194681-29194938 | Common:2; Rare:63 | ||||
| chr7:29989727-29989898 | Rare:68 | ||||
| chr7:30026624-30026828 | Rare:48 | ||||
| chr7:30478681-30478945 | Common:5; Rare:92; Clinvar:1 | ||||
| chr7:30504740-30505103 | Common:3; Rare:122 | ||||
| chr7:30594705-30594933 | Common:4; Rare:100; Clinvar:6; Clinvar (benign):7 |