Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:74592462-74592692 | Common:1; Rare:71 | ||||
chr11:74748626-74748973 | Common:3; Rare:111 | ||||
chr11:74749105-74749568 | Common:5; Rare:127 | ||||
chr11:74948979-74949434 | Common:8; Rare:143 | ||||
chr11:74949921-74950013 | Rare:24 | ||||
chr11:74988634-74989126 | Rare:129 | ||||
chr11:75100336-75100661 | Rare:50 | ||||
chr11:75399403-75399638 | Common:5; Rare:100 | ||||
chr11:75430152-75430353 | Common:1; Rare:85 | ||||
chr11:75525782-75526101 | Common:2; Rare:95 | ||||
chr11:75561969-75562164 | Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
chr11:75562219-75562415 | Common:1; Rare:40; Clinvar (benign):1 | ||||
chr11:75562620-75562948 | Common:1; Rare:74 | ||||
chr11:75563257-75563331 | Rare:13 | ||||
chr11:75768332-75768839 | Common:4; Rare:152 |