| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27662795-27663152 | Common:6; Rare:126 | ||||
| chr7:27740070-27740221 | Common:5; Rare:43 | ||||
| chr7:28180570-28180793 | Common:1; Rare:66 | ||||
| chr7:28435406-28435435 | Rare:2 | ||||
| chr7:28686019-28686104 | Rare:22 | ||||
| chr7:28958273-28958471 | Rare:54 | ||||
| chr7:28958607-28958679 | Common:1; Rare:17 | ||||
| chr7:29563646-29563889 | Common:1; Rare:62 | ||||
| chr7:29989639-29990058 | Rare:148 | ||||
| chr7:30026609-30026994 | Common:1; Rare:93 | ||||
| chr7:30028209-30028497 | Common:1; Rare:103 | ||||
| chr7:30504594-30504658 | Rare:24 | ||||
| chr7:30504663-30505041 | Common:3; Rare:127 | ||||
| chr7:30594702-30595149 | Common:9; Rare:192; Clinvar:11; Clinvar (benign):17 | ||||
| chr7:30983747-30983937 | Common:1; Rare:33 |