Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:42302416-42302500 | Rare:19 | ||||
chr19:43527178-43527315 | Common:4; Rare:53; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr19:43575465-43575850 | Common:2; Rare:100 | ||||
chr19:43619577-43619861 | Common:3; Rare:85 | ||||
chr19:43670127-43670292 | Common:2; Rare:39 | ||||
chr19:43754901-43755102 | Common:3; Rare:69 | ||||
chr19:44141483-44141598 | Common:2; Rare:17 | ||||
chr19:44164840-44165140 | Common:1; Rare:74 | ||||
chr19:44356681-44356851 | Common:1; Rare:33 | ||||
chr19:44500512-44500650 | Common:3; Rare:39 | ||||
chr19:44643795-44643918 | Rare:37 | ||||
chr19:44808972-44809119 | Rare:55 | ||||
chr19:44955217-44955410 | Common:2; Rare:53 | ||||
chr19:45038960-45039090 | Rare:42 | ||||
chr19:45370536-45370731 | Common:2; Rare:61 |