Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15526578-15526924 | Common:2; Rare:112 | ||||
chr1:16018039-16018294 | Common:5; Rare:77 | ||||
chr1:16352420-16352615 | Common:3; Rare:102 | ||||
chr1:16440617-16440774 | Rare:54 | ||||
chr1:17053976-17054362 | Common:3; Rare:116; Clinvar:12; Clinvar (benign):10 | ||||
chr1:19210234-19210422 | Rare:73 | ||||
chr1:19251498-19251866 | Common:6; Rare:122 | ||||
chr1:19312013-19312346 | Common:8; Rare:157 | ||||
chr1:19485435-19485765 | Common:1; Rare:124 | ||||
chr1:20508072-20508216 | Common:2; Rare:50 | ||||
chr1:20661346-20661663 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787196-20787470 | Rare:129 | ||||
chr1:21345463-21345655 | Common:2; Rare:75 | ||||
chr1:23559394-23559643 | Common:1; Rare:108 | ||||
chr1:23691718-23691829 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):1 |