Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:105487141-105487242 | Rare:39 | ||||
chr15:23039546-23039695 | Common:1; Rare:59 | ||||
chr15:23565481-23565697 | Common:2; Rare:61 | ||||
chr15:23566170-23566359 | Rare:97; Clinvar (pathogenic):1 | ||||
chr15:23687269-23687425 | Common:1; Rare:53 | ||||
chr15:24823515-24823697 | Rare:44 | ||||
chr15:24856489-24856610 | Common:1; Rare:32 | ||||
chr15:25438984-25439227 | Common:2; Rare:91 | ||||
chr15:30903779-30903974 | Rare:51 | ||||
chr15:31870603-31870953 | Rare:114 | ||||
chr15:32030359-32030530 | Common:6; Rare:47 | ||||
chr15:32615096-32615624 | Common:7; Rare:132 | ||||
chr15:32641629-32641771 | Common:2; Rare:34 | ||||
chr15:33310405-33311031 | Common:5; Rare:180 | ||||
chr15:34101835-34102117 | Common:1; Rare:58 |