Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:44392671-44392977 | Common:1; Rare:73 | ||||
chr3:45595767-45595867 | Rare:36 | ||||
chr3:48917980-48918247 | Rare:47 | ||||
chr3:49101684-49101858 | Rare:51; Clinvar (benign):6 | ||||
chr3:49132114-49132375 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr3:49357368-49357452 | Common:2; Rare:33; Clinvar (benign):1 | ||||
chr3:49357485-49357748 | Rare:103 | ||||
chr3:50358452-50358606 | Rare:52 | ||||
chr3:51393407-51393622 | Rare:70 | ||||
chr3:52199028-52199359 | Rare:81 | ||||
chr3:52502003-52502201 | Rare:56 | ||||
chr3:52512432-52512618 | Common:1; Rare:44 | ||||
chr3:52691367-52691618 | Rare:54 | ||||
chr3:52781842-52782065 | Common:1; Rare:64 | ||||
chr3:52795542-52795671 | Common:2; Rare:48 |