Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:35399939-35400151 | Rare:68 | ||||
chr22:35648309-35648566 | Common:1; Rare:44 | ||||
chr22:36239500-36239665 | Rare:53 | ||||
chr22:36387811-36388170 | Common:2; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
chr22:36481562-36481729 | Common:2; Rare:45 | ||||
chr22:36507031-36507163 | Common:2; Rare:46 | ||||
chr22:36529083-36529531 | Common:6; Rare:139 | ||||
chr22:37019411-37019781 | Common:5; Rare:106 | ||||
chr22:37560331-37560547 | Common:1; Rare:73 | ||||
chr22:37676168-37676188 | Rare:1 | ||||
chr22:37805568-37805814 | Rare:79 | ||||
chr22:37807810-37807958 | Common:2; Rare:51 | ||||
chr22:37849316-37849480 | Rare:93 | ||||
chr22:37953587-37953800 | Rare:82 | ||||
chr22:37984535-37984683 | Rare:37 |