Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:36158619-36158743 | Common:1; Rare:26 | ||||
chr22:36288726-36289152 | Common:2; Rare:124; Clinvar:3; Clinvar (benign):6 | ||||
chr22:36523933-36524169 | Common:4; Rare:55 | ||||
chr22:37806228-37806482 | Common:3; Rare:50 | ||||
chr22:38738264-38738376 | Rare:30 | ||||
chr22:38741492-38741845 | Common:3; Rare:79; Clinvar (benign):1 | ||||
chr22:39405500-39405732 | Common:1; Rare:48 | ||||
chr22:41220603-41220663 | Common:1; Rare:12 | ||||
chr22:41522700-41522916 | Rare:45; Clinvar (pathogenic):1 | ||||
chr22:41522983-41523272 | Rare:83 | ||||
chr22:41529282-41529595 | Common:1; Rare:82 | ||||
chr22:42587986-42588173 | Common:2; Rare:40 | ||||
chr22:42879222-42879378 | Common:2; Rare:31 | ||||
chr22:46069885-46070056 | Rare:41 | ||||
chr22:46085753-46086044 | Common:2; Rare:73 |