Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:21665934-21666032 | Rare:22 | ||||
chr22:23894213-23894516 | Common:3; Rare:114 | ||||
chr22:24555913-24556048 | Rare:41 | ||||
chr22:26483772-26484007 | Common:6; Rare:98; Clinvar:5; Clinvar (benign):1 | ||||
chr22:26512447-26512550 | Common:1; Rare:48 | ||||
chr22:27919195-27919504 | Common:5; Rare:139 | ||||
chr22:28741793-28742052 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
chr22:28800564-28800703 | Common:2; Rare:41 | ||||
chr22:29267969-29268348 | Common:2; Rare:113 | ||||
chr22:30356868-30356985 | Common:1; Rare:38 | ||||
chr22:31496409-31496542 | Common:1; Rare:33 | ||||
chr22:36529077-36529473 | Common:5; Rare:121 | ||||
chr22:37849293-37849462 | Rare:103 | ||||
chr22:38681817-38682009 | Common:1; Rare:82 | ||||
chr22:39319596-39319768 | Common:3; Rare:81 |