Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:27150918-27151038 | Rare:29 | ||||
chr7:27156192-27156367 | Common:1; Rare:70 | ||||
chr7:27157993-27158081 | Rare:15 | ||||
chr7:27179815-27179987 | Rare:64 | ||||
chr7:27185183-27185405 | Common:1; Rare:85 | ||||
chr7:27740069-27740218 | Common:5; Rare:41 | ||||
chr7:29563679-29563896 | Rare:56 | ||||
chr7:30026615-30026862 | Rare:60 | ||||
chr7:30504780-30505090 | Common:2; Rare:97 | ||||
chr7:30594733-30595090 | Common:6; Rare:169; Clinvar:9; Clinvar (benign):13 | ||||
chr7:32490361-32490470 | Rare:35 | ||||
chr7:32495240-32495598 | Common:1; Rare:91 | ||||
chr7:33129232-33129586 | Common:5; Rare:99 | ||||
chr7:35695133-35695248 | Rare:40 | ||||
chr7:35800721-35801252 | Common:2; Rare:201 |