Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40257904-40258326 | Common:4; Rare:122; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40316090-40316168 | Rare:19 | ||||
chr1:40344695-40344879 | Rare:28 | ||||
chr1:40374006-40374215 | Rare:51 | ||||
chr1:40374362-40374483 | Rare:21 | ||||
chr1:40374495-40374530 | Rare:4 | ||||
chr1:40374566-40375150 | Common:13; Rare:97 | ||||
chr1:40393358-40393376 | Rare:5 | ||||
chr1:40396543-40396835 | Common:1; Rare:36 | ||||
chr1:40508626-40508812 | Common:6; Rare:57 | ||||
chr1:40531514-40531721 | Common:1; Rare:53 | ||||
chr1:40691375-40691864 | Common:3; Rare:197 | ||||
chr1:40691945-40692025 | Rare:24 | ||||
chr1:40692027-40692137 | Rare:46 | ||||
chr1:40862350-40862568 | Common:5; Rare:72 |