Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:20917238-20917466 | Rare:89 | ||||
chr22:20982196-20982329 | Common:2; Rare:30; Clinvar (benign):2 | ||||
chr22:21002088-21002227 | Common:3; Rare:52 | ||||
chr22:21952824-21953174 | Common:3; Rare:94 | ||||
chr22:23750972-23751206 | Common:1; Rare:80 | ||||
chr22:23894095-23894581 | Common:5; Rare:160 | ||||
chr22:23979724-23979916 | |||||
chr22:24555044-24555389 | Common:4; Rare:124 | ||||
chr22:24555884-24556071 | Rare:55 | ||||
chr22:24952616-24952732 | Rare:35 | ||||
chr22:26483746-26483880 | Common:4; Rare:60; Clinvar:6; Clinvar (benign):1 | ||||
chr22:26512428-26512550 | Common:1; Rare:55 | ||||
chr22:26590077-26590214 | Common:3; Rare:56 | ||||
chr22:27919187-27919538 | Common:5; Rare:158 | ||||
chr22:28741800-28742074 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 |