Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:53869293-53869810 | Common:3; Rare:137 | ||||
chr19:53879380-53879810 | Common:4; Rare:97 | ||||
chr19:53881334-53881561 | Rare:46 | ||||
chr19:53881947-53882336 | Common:1; Rare:92; Clinvar:2 | ||||
chr19:53882621-53882854 | Rare:44 | ||||
chr19:53909128-53909572 | Common:1; Rare:111 | ||||
chr19:53962965-53963140 | Common:1; Rare:34 | ||||
chr19:54102669-54103142 | Common:5; Rare:121 | ||||
chr19:54115106-54115463 | Common:1; Rare:96; Clinvar (benign):1 | ||||
chr19:54115539-54115802 | Common:2; Rare:67; Clinvar:6 | ||||
chr19:54137823-54137981 | Rare:35 | ||||
chr19:54144039-54144333 | Common:1; Rare:64 | ||||
chr19:54159673-54160153 | Common:1; Rare:156 | ||||
chr19:54164711-54164906 | Common:2; Rare:33 | ||||
chr19:54173115-54173434 | Common:4; Rare:78 |