Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234608184-234608306 | Rare:41 | ||||
chr1:235128750-235129025 | Rare:111 | ||||
chr1:235328791-235329014 | Common:1; Rare:72 | ||||
chr1:235866858-235867132 | Common:3; Rare:82 | ||||
chr1:236065018-236065356 | Common:3; Rare:123; Clinvar (pathogenic):1 | ||||
chr1:236281956-236282219 | Common:6; Rare:71 | ||||
chr1:236523861-236524041 | Common:2; Rare:46 | ||||
chr1:239386245-239386684 | Common:2; Rare:73 | ||||
chr1:239386705-239387004 | Common:1; Rare:94 | ||||
chr1:241519667-241519977 | Common:2; Rare:100; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr1:241848092-241848255 | Common:2; Rare:33 | ||||
chr1:242449378-242449523 | Rare:32 | ||||
chr1:243255047-243255433 | Common:1; Rare:92 | ||||
chr1:243255755-243256113 | Rare:99; Clinvar:4 | ||||
chr1:244051128-244051408 | Rare:41 |