Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:32127444-32127620 | Rare:43 | ||||
chr17:35567869-35568156 | Common:3; Rare:90 | ||||
chr17:42422720-42422906 | Rare:74; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr17:43315658-43315916 | Common:6; Rare:108 | ||||
chr17:43388308-43388379 | Rare:13 | ||||
chr17:45247776-45247963 | Common:1; Rare:32 | ||||
chr17:47492466-47492493 | Common:1; Rare:12 | ||||
chr17:48961643-48961781 | Common:1; Rare:40 | ||||
chr17:50189865-50190074 | Common:1; Rare:60; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:58659295-58659556 | Common:3; Rare:88 | ||||
chr17:64145750-64145975 | Common:2; Rare:59 | ||||
chr17:64837133-64837268 | Common:1; Rare:32 | ||||
chr17:64975559-64975727 | Common:1; Rare:62 | ||||
chr17:68101486-68101563 | Common:2; Rare:38 | ||||
chr17:68695100-68695398 | Common:5; Rare:52 |