Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:41522612-41522862 | Common:2; Rare:54 | ||||
chr22:41522967-41523272 | Rare:93; Clinvar:2 | ||||
chr22:42581975-42582327 | Common:6; Rare:117 | ||||
chr22:42601135-42601229 | Rare:21 | ||||
chr22:42623796-42623964 | Rare:51; Clinvar (pathogenic):1 | ||||
chr22:42933744-42934075 | Common:4; Rare:63 | ||||
chr22:42937534-42937712 | Rare:30 | ||||
chr22:46069832-46070056 | Rare:47 | ||||
chr22:46080056-46080348 | Common:1; Rare:94 | ||||
chr22:46085769-46086068 | Common:2; Rare:77 | ||||
chr22:49934232-49934423 | Common:2; Rare:38 | ||||
chr22:49962492-49962813 | Common:4; Rare:123 | ||||
chr22:49970818-49971072 | Common:1; Rare:59 | ||||
chr22:50267686-50267858 | Common:1; Rare:65 | ||||
chr22:50314502-50314685 | Common:1; Rare:77 |