Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44187169-44187274 | Rare:30 | ||||
chr17:44221226-44221302 | Rare:21 | ||||
chr17:44324765-44324963 | Common:2; Rare:70 | ||||
chr17:44503374-44503556 | Rare:74 | ||||
chr17:44947658-44947930 | Common:1; Rare:77 | ||||
chr17:45060958-45061339 | Common:3; Rare:98 | ||||
chr17:45490719-45490863 | Rare:50 | ||||
chr17:46923048-46923193 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):7 | ||||
chr17:47189235-47189563 | Rare:82 | ||||
chr17:47253617-47253931 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):4 | ||||
chr17:47831501-47831649 | Rare:40 | ||||
chr17:47941354-47941702 | Rare:93; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048039-48048405 | Common:1; Rare:100 | ||||
chr17:48048602-48048797 | Common:4; Rare:26 | ||||
chr17:48610682-48611078 | Common:5; Rare:124 |