Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:29205777-29206031 | Common:1; Rare:69 | ||||
chr22:29267894-29267921 | Rare:7 | ||||
chr22:29267926-29267939 | Rare:3 | ||||
chr22:29267943-29268339 | Common:2; Rare:115 | ||||
chr22:29767057-29767401 | Common:4; Rare:108 | ||||
chr22:29838204-29838426 | Common:3; Rare:73 | ||||
chr22:30326886-30327188 | Common:1; Rare:108 | ||||
chr22:30356855-30357048 | Common:2; Rare:61 | ||||
chr22:30607047-30607236 | Common:3; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
chr22:31081106-31081351 | Common:1; Rare:68 | ||||
chr22:31160142-31160269 | Rare:46 | ||||
chr22:31290667-31290906 | Rare:99 | ||||
chr22:31292425-31292499 | Rare:17 | ||||
chr22:31496446-31496567 | Common:1; Rare:32 | ||||
chr22:31630809-31630976 | Common:5; Rare:42 |