Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:6009023-6009323 | Common:3; Rare:128; Clinvar:6; Clinvar (benign):14 | ||||
chr7:6577387-6577481 | Rare:29 | ||||
chr7:12687428-12687651 | Common:5; Rare:71 | ||||
chr7:16465730-16465960 | Rare:38 | ||||
chr7:23105655-23105819 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
chr7:23181793-23182083 | Common:2; Rare:111 | ||||
chr7:23470362-23470560 | Rare:58 | ||||
chr7:23531958-23532116 | Common:1; Rare:62 | ||||
chr7:24757406-24757552 | Common:1; Rare:47 | ||||
chr7:25125215-25125428 | Rare:90; Clinvar:3 | ||||
chr7:26200661-26200953 | Common:2; Rare:152 | ||||
chr7:26201211-26201805 | Common:2; Rare:271 | ||||
chr7:26864581-26864840 | Common:3; Rare:80 | ||||
chr7:27172796-27173074 | Rare:66 | ||||
chr7:27179847-27179987 | Rare:52 |