Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235866849-235867074 | Common:3; Rare:68 | ||||
chr1:236064972-236065363 | Common:4; Rare:139; Clinvar (pathogenic):1 | ||||
chr1:236523924-236524036 | Common:1; Rare:29 | ||||
chr1:236604456-236604588 | Common:4; Rare:41 | ||||
chr1:239386507-239386592 | Rare:14 | ||||
chr1:241848094-241848248 | Common:2; Rare:32 | ||||
chr1:243255040-243255420 | Common:1; Rare:89 | ||||
chr1:243255776-243256136 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451844-244452166 | Common:1; Rare:115 | ||||
chr1:244461286-244461317 | Common:1; Rare:9 | ||||
chr1:244652510-244652570 | Common:2; Rare:17 | ||||
chr1:244835192-244835333 | Rare:59 | ||||
chr1:244835580-244835729 | Common:2; Rare:66; Clinvar (benign):4 | ||||
chr1:244863940-244863977 | Rare:9; Clinvar (benign):1 | ||||
chr1:244864391-244864691 | Rare:118 |