Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25819898-25820013 | Common:2; Rare:34 | ||||
chr1:25859359-25859549 | Common:3; Rare:80 | ||||
chr1:26234005-26234252 | Common:1; Rare:88 | ||||
chr1:26279933-26280158 | Rare:127 | ||||
chr1:26432098-26432414 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472312-26472574 | Common:4; Rare:100 | ||||
chr1:26900438-26900524 | Rare:33 | ||||
chr1:28505801-28506050 | Common:2; Rare:92 | ||||
chr1:28643023-28643159 | Rare:57 | ||||
chr1:28736753-28737010 | Common:1; Rare:94 | ||||
chr1:28737719-28737750 | Rare:10 | ||||
chr1:31296743-31297094 | Common:5; Rare:114 | ||||
chr1:31373052-31373272 | Rare:63 | ||||
chr1:32072799-32072942 | Rare:39 | ||||
chr1:32222335-32222547 | Rare:85 |