Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:26672745-26672839 | Rare:21 | ||||
chr22:29481010-29481125 | Common:1; Rare:48 | ||||
chr22:30969043-30969278 | Common:2; Rare:66 | ||||
chr22:35836389-35836674 | Rare:64 | ||||
chr22:35894936-35895151 | Common:1; Rare:50 | ||||
chr22:35914611-35914788 | Rare:47 | ||||
chr22:36288844-36289135 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):3 | ||||
chr22:36331570-36331746 | Common:2; Rare:32 | ||||
chr22:36455080-36455379 | Common:4; Rare:91 | ||||
chr22:38397322-38397453 | Rare:41 | ||||
chr22:38463443-38463620 | Rare:41 | ||||
chr22:38486323-38486613 | Rare:70 | ||||
chr22:38992860-38993006 | Common:1; Rare:31 | ||||
chr22:39243970-39244161 | Rare:65 | ||||
chr22:39521507-39521813 | Common:2; Rare:147 |