Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:89560560-89560717 | Rare:65 | ||||
chr16:89657584-89658159 | Common:5; Rare:281; Clinvar (benign):1 | ||||
chr16:89686574-89686713 | Common:6; Rare:67 | ||||
chr16:89686904-89686960 | Rare:22 | ||||
chr16:89720865-89721037 | Common:1; Rare:54 | ||||
chr16:89873490-89873797 | Common:2; Rare:141 | ||||
chr16:89972476-89972669 | Common:1; Rare:71 | ||||
chr16:90022594-90022716 | Common:1; Rare:51 | ||||
chr17:352772-352830 | Common:1; Rare:15 | ||||
chr17:714687-714893 | Common:3; Rare:75; Clinvar (benign):1 | ||||
chr17:752259-752309 | Rare:13 | ||||
chr17:1400048-1400381 | Common:3; Rare:141 | ||||
chr17:1491612-1491818 | Common:1; Rare:63 | ||||
chr17:1516582-1516960 | Common:2; Rare:134 | ||||
chr17:1762585-1762826 | Common:3; Rare:47 |