Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:58513336-58513577 | Rare:37 | ||||
chr17:58513971-58514086 | Rare:19 | ||||
chr17:58517830-58518185 | Common:1; Rare:81 | ||||
chr17:58518256-58518401 | Rare:23 | ||||
chr17:58692549-58692706 | Common:1; Rare:83; Clinvar:21; Clinvar (benign):20 | ||||
chr17:59106488-59106999 | Common:3; Rare:156; Clinvar:7; Clinvar (benign):4 | ||||
chr17:59155122-59155523 | Common:2; Rare:96 | ||||
chr17:59155557-59155710 | Rare:45 | ||||
chr17:59220324-59220765 | Common:4; Rare:136 | ||||
chr17:59221073-59221198 | Rare:28 | ||||
chr17:59331491-59331758 | Common:2; Rare:88 | ||||
chr17:59565343-59565730 | Common:2; Rare:136 | ||||
chr17:59619253-59619318 | Rare:15 | ||||
chr17:59619480-59620167 | Common:3; Rare:230 | ||||
chr17:59707397-59707727 | Common:3; Rare:90; Clinvar (benign):3 |