Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37594767-37594868 | Rare:26 | ||||
chr19:37932445-37932644 | Common:2; Rare:37 | ||||
chr19:38315883-38316256 | Common:1; Rare:105 | ||||
chr19:38647372-38647748 | Common:3; Rare:132 | ||||
chr19:38831755-38832055 | Common:4; Rare:92; Clinvar (benign):1 | ||||
chr19:38899586-38900018 | Rare:127 | ||||
chr19:38930723-38930992 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39390850-39390933 | Rare:36 | ||||
chr19:39391021-39391418 | Common:1; Rare:158 | ||||
chr19:39435861-39436163 | Common:6; Rare:110 | ||||
chr19:39445519-39445719 | Common:1; Rare:49 | ||||
chr19:39480695-39480921 | Common:3; Rare:120; Clinvar (pathogenic):1 | ||||
chr19:39846312-39846487 | Common:1; Rare:83 | ||||
chr19:39970900-39971215 | Common:4; Rare:93 | ||||
chr19:40056168-40056253 | Rare:14 |