Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:55587649-55587699 | Rare:13 | ||||
chr18:55588095-55588339 | Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
chr18:55589710-55589908 | Rare:54 | ||||
chr18:56651123-56651430 | Common:4; Rare:81 | ||||
chr18:56651595-56651681 | Common:3; Rare:22 | ||||
chr18:57621710-57621947 | Common:2; Rare:85 | ||||
chr18:58671230-58671608 | Common:4; Rare:169; Clinvar (benign):1 | ||||
chr18:58862844-58863015 | Rare:32 | ||||
chr18:58864065-58864419 | Common:2; Rare:93 | ||||
chr18:58864760-58864885 | Rare:28 | ||||
chr18:58920497-58920807 | Common:2; Rare:63 | ||||
chr18:59139694-59139944 | Common:2; Rare:66 | ||||
chr18:59358521-59358818 | Common:1; Rare:79 | ||||
chr18:59899614-59900073 | Common:4; Rare:139 | ||||
chr18:61894439-61894573 | Common:2; Rare:38 |