Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44775835-44776155 | Common:2; Rare:115 | ||||
chr1:44843227-44843434 | Rare:56 | ||||
chr1:44986543-44986694 | Common:2; Rare:25; Clinvar (benign):1 | ||||
chr1:45010929-45011148 | Common:2; Rare:65 | ||||
chr1:45012055-45012262 | Common:1; Rare:74; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45340103-45340174 | Rare:27 | ||||
chr1:45340388-45340466 | Common:1; Rare:18; Clinvar:1 | ||||
chr1:45500019-45500356 | Common:2; Rare:80; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521818-45521984 | Common:1; Rare:65 | ||||
chr1:45550741-45551076 | Common:3; Rare:82 | ||||
chr1:45583940-45584114 | Rare:68 | ||||
chr1:45686503-45686651 | Rare:47 | ||||
chr1:45687041-45687317 | Common:1; Rare:75 | ||||
chr1:45688104-45688240 | Common:1; Rare:44 | ||||
chr1:45750615-45750808 | Rare:72 |