Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:58219220-58219488 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
chr17:58352111-58352275 | Common:1; Rare:70 | ||||
chr17:58487900-58488010 | Rare:29 | ||||
chr17:58692501-58692663 | Common:2; Rare:89; Clinvar:9; Clinvar (benign):19 | ||||
chr17:59155168-59155436 | Common:2; Rare:66 | ||||
chr17:59565371-59565661 | Common:2; Rare:107 | ||||
chr17:59619578-59619923 | Common:3; Rare:124 | ||||
chr17:59707394-59707537 | Common:1; Rare:36; Clinvar (benign):3 | ||||
chr17:59707606-59707744 | Common:1; Rare:39 | ||||
chr17:59892882-59893123 | Rare:70 | ||||
chr17:59964705-59964833 | Common:2; Rare:57 | ||||
chr17:60525920-60526310 | Common:2; Rare:132 | ||||
chr17:60600009-60600229 | Common:3; Rare:78 | ||||
chr17:63550196-63550501 | Common:2; Rare:68 | ||||
chr17:63600832-63600910 | Rare:21; Clinvar:1 |