Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:55214644-55214905 | Common:2; Rare:79 | ||||
chr1:56645258-56645394 | Common:1; Rare:54 | ||||
chr1:57423985-57424338 | Common:5; Rare:94 | ||||
chr1:58783977-58784391 | Common:1; Rare:113 | ||||
chr1:59296611-59296843 | Common:11; Rare:61 | ||||
chr1:59814485-59814810 | Common:3; Rare:97 | ||||
chr1:61725013-61725228 | Common:1; Rare:101 | ||||
chr1:61742211-61742515 | Rare:74 | ||||
chr1:62435783-62435995 | Rare:41 | ||||
chr1:62436245-62436364 | Common:2; Rare:38 | ||||
chr1:62436985-62437165 | Common:1; Rare:56 | ||||
chr1:62688260-62688553 | Common:1; Rare:112; Clinvar:1 | ||||
chr1:62783549-62783856 | Common:1; Rare:56 | ||||
chr1:62784041-62784193 | Rare:62 | ||||
chr1:63367476-63367686 | Rare:66; Clinvar (benign):1 |