Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:120176354-120176621 | Common:1; Rare:56 | ||||
chr1:145823937-145824265 | Rare:117 | ||||
chr1:145918686-145919037 | Common:2; Rare:77 | ||||
chr1:145927418-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145964575-145964749 | Rare:44 | ||||
chr1:147172450-147172817 | Common:1; Rare:93 | ||||
chr1:149812267-149812609 | Common:3; Rare:135 | ||||
chr1:149813687-149813958 | Common:2; Rare:77 | ||||
chr1:149861153-149861417 | |||||
chr1:149886621-149887034 | Common:3; Rare:159 | ||||
chr1:149887895-149888215 | Rare:98 | ||||
chr1:149927743-149927900 | Common:1; Rare:63; Clinvar (benign):5 | ||||
chr1:150010697-150010826 | Common:1; Rare:32 | ||||
chr1:150067680-150067860 | Rare:58 | ||||
chr1:150235935-150236368 | Common:1; Rare:96 |