Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38852305-38852480 | Rare:47 | ||||
chr19:38878249-38878300 | Rare:7 | ||||
chr19:38893484-38893707 | Common:3; Rare:55 | ||||
chr19:38899528-38900079 | Rare:165 | ||||
chr19:38930715-38930996 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
chr19:38975676-38975857 | Common:1; Rare:45 | ||||
chr19:39342367-39342527 | Common:2; Rare:54 | ||||
chr19:39390696-39390801 | Rare:32 | ||||
chr19:39390845-39390957 | Rare:41 | ||||
chr19:39390963-39391492 | Common:1; Rare:202 | ||||
chr19:39406673-39406955 | Rare:106 | ||||
chr19:39407503-39407925 | Common:1; Rare:118 | ||||
chr19:39435848-39436142 | Common:6; Rare:109 | ||||
chr19:39445426-39445880 | Common:3; Rare:140 | ||||
chr19:39480731-39480925 | Common:3; Rare:105; Clinvar (pathogenic):1 |