Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:58577253-58577496 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
chr1:58700048-58700131 | Common:1; Rare:37 | ||||
chr1:58783722-58784077 | Common:1; Rare:99 | ||||
chr1:58784302-58784384 | Common:1; Rare:22 | ||||
chr1:59296520-59297103 | Common:14; Rare:163 | ||||
chr1:61076963-61077283 | Common:3; Rare:79 | ||||
chr1:61725021-61725228 | Common:1; Rare:97 | ||||
chr1:61742369-61742551 | Rare:54 | ||||
chr1:62436256-62436364 | Common:2; Rare:36 | ||||
chr1:62436465-62437109 | Common:1; Rare:156 | ||||
chr1:62688274-62688500 | Common:1; Rare:94 | ||||
chr1:62784069-62784185 | Rare:48 | ||||
chr1:63523179-63523589 | Common:3; Rare:105 | ||||
chr1:63593148-63593472 | Rare:113; Clinvar (benign):1 | ||||
chr1:64841245-64841569 | Rare:77; Clinvar:2 |