Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:58415577-58415609 | Rare:7 | ||||
chr17:58417486-58417868 | Common:1; Rare:71 | ||||
chr17:58487849-58488068 | Rare:48 | ||||
chr17:58514048-58514187 | Rare:29 | ||||
chr17:58514516-58514735 | Rare:50 | ||||
chr17:58517760-58517934 | Common:1; Rare:37 | ||||
chr17:58518256-58518612 | Rare:52 | ||||
chr17:58692449-58692892 | Common:3; Rare:203; Clinvar:36; Clinvar (benign):34; Clinvar (pathogenic):3 | ||||
chr17:59106251-59106482 | Common:1; Rare:64 | ||||
chr17:59106610-59107295 | Common:5; Rare:200; Clinvar:6; Clinvar (benign):4 | ||||
chr17:59154870-59155066 | Rare:56 | ||||
chr17:59155141-59155334 | Common:1; Rare:53 | ||||
chr17:59155555-59155832 | Rare:70 | ||||
chr17:59209310-59209423 | Common:1; Rare:12 | ||||
chr17:59209911-59210166 | Common:1; Rare:93 |