| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56051424-56051863 | Common:1; Rare:169; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56051943-56051985 | Rare:9 | ||||
| chr7:56106380-56106681 | Common:8; Rare:111 | ||||
| chr7:64563038-64563223 | Common:2; Rare:49 | ||||
| chr7:66114767-66114895 | Common:1; Rare:64 | ||||
| chr7:66115238-66115353 | Rare:24 | ||||
| chr7:66681972-66682165 | Common:5; Rare:83 | ||||
| chr7:66995473-66995763 | Rare:78 | ||||
| chr7:66996589-66996871 | Common:2; Rare:57 | ||||
| chr7:72828159-72828511 | Rare:94 | ||||
| chr7:73683425-73683622 | Common:3; Rare:77 | ||||
| chr7:73738776-73739072 | Common:1; Rare:93 | ||||
| chr7:73842472-73842716 | Common:6; Rare:45 | ||||
| chr7:74174110-74174393 | Common:1; Rare:147 | ||||
| chr7:74254346-74254528 | Rare:84 |