Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:1806073-1806314 | Common:2; Rare:91; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr4:3206161-3206293 | Common:1; Rare:30 | ||||
chr4:3447986-3448234 | Common:5; Rare:102 | ||||
chr4:6673825-6673969 | Common:7; Rare:76 | ||||
chr4:6709260-6709318 | Rare:21 | ||||
chr4:6730682-6730875 | Common:1; Rare:44 | ||||
chr4:6733614-6733951 | Common:4; Rare:84 | ||||
chr4:6753161-6753301 | Common:1; Rare:30 | ||||
chr4:38868349-38868454 | Rare:19 | ||||
chr4:38904363-38904526 | Common:3; Rare:30 | ||||
chr4:38950755-38950997 | Common:5; Rare:36 | ||||
chr4:39469824-39469912 | Rare:12 | ||||
chr4:39469915-39470082 | Rare:47; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr4:39472385-39472619 | Rare:32 | ||||
chr4:41934174-41934403 | Rare:47 |