Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173824325-173824708 | Rare:78; Clinvar:1 | ||||
chr1:173867966-173868169 | Common:1; Rare:79 | ||||
chr1:174999312-174999480 | Common:1; Rare:45 | ||||
chr1:174999620-175000114 | Common:1; Rare:148 | ||||
chr1:175023409-175023506 | Common:1; Rare:29 | ||||
chr1:178725131-178725320 | Common:10; Rare:72 | ||||
chr1:179081917-179082114 | Common:1; Rare:62 | ||||
chr1:179143067-179143238 | Rare:29 | ||||
chr1:179882067-179882302 | Common:1; Rare:55 | ||||
chr1:179882472-179882843 | Rare:172; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954482-179954817 | Common:3; Rare:82 | ||||
chr1:180154662-180154904 | Common:3; Rare:82 | ||||
chr1:180502529-180502697 | Rare:71 | ||||
chr1:181088521-181088703 | Rare:62 | ||||
chr1:182839553-182839730 | Common:2; Rare:78 |