Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:58219216-58219376 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):4 | ||||
chr17:58352125-58352368 | Common:4; Rare:113 | ||||
chr17:58517830-58518298 | Common:1; Rare:108 | ||||
chr17:58692549-58692678 | Common:1; Rare:73; Clinvar:15; Clinvar (benign):20 | ||||
chr17:59106689-59106977 | Common:2; Rare:97; Clinvar:5; Clinvar (benign):3 | ||||
chr17:59154979-59155677 | Common:2; Rare:193 | ||||
chr17:59331491-59331787 | Common:2; Rare:98 | ||||
chr17:59565469-59565700 | Common:1; Rare:87 | ||||
chr17:59619518-59619629 | Common:1; Rare:33 | ||||
chr17:59619631-59620171 | Common:2; Rare:187 | ||||
chr17:59647211-59647661 | Rare:73 | ||||
chr17:59683783-59683985 | Rare:36 | ||||
chr17:59707397-59707539 | Common:1; Rare:35; Clinvar (benign):3 | ||||
chr17:59837617-59838009 | Rare:58 | ||||
chr17:59838423-59838927 | Common:1; Rare:87 |