Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:241519634-241520042 | Common:3; Rare:123; Clinvar:13; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
chr1:241531757-241531858 | Rare:24 | ||||
chr1:241532019-241532311 | Common:2; Rare:60 | ||||
chr1:241639527-241639909 | Common:5; Rare:95 | ||||
chr1:241640102-241640131 | Rare:10 | ||||
chr1:241640224-241640615 | Common:7; Rare:136 | ||||
chr1:241847757-241848272 | Common:5; Rare:133 | ||||
chr1:243253418-243253484 | Rare:10 | ||||
chr1:243254356-243254725 | Common:4; Rare:86 | ||||
chr1:243254935-243255457 | Common:1; Rare:124 | ||||
chr1:243255741-243256163 | Common:1; Rare:123; Clinvar:4; Clinvar (benign):1 | ||||
chr1:243269517-243269681 | Common:2; Rare:30 | ||||
chr1:243850461-243850570 | Rare:37 | ||||
chr1:243851007-243851195 | Common:2; Rare:72 | ||||
chr1:244048014-244048737 | Common:2; Rare:220 |