Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:197949893-197950251 | Common:4; Rare:112; Clinvar (benign):2 | ||||
chr3:197959975-197960267 | Common:1; Rare:106 | ||||
chr4:337482-337833 | Common:1; Rare:91 | ||||
chr4:499100-499315 | Common:3; Rare:88 | ||||
chr4:673842-673952 | Rare:47 | ||||
chr4:674246-674585 | Common:3; Rare:158 | ||||
chr4:689152-689244 | Common:2; Rare:25 | ||||
chr4:932250-932487 | Common:2; Rare:93 | ||||
chr4:1113544-1113576 | Rare:9 | ||||
chr4:1289662-1289911 | Common:1; Rare:80 | ||||
chr4:2041912-2042017 | Common:1; Rare:41 | ||||
chr4:2468878-2469167 | Common:4; Rare:108 | ||||
chr4:2843689-2844000 | Common:3; Rare:114 | ||||
chr4:2934777-2934954 | Common:5; Rare:84 | ||||
chr4:4248179-4248261 | Common:3; Rare:39 |