Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41869665-41869743 | Rare:27 | ||||
chr19:41869745-41869875 | Common:2; Rare:34; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:42106837-42106839 | |||||
chr19:42150964-42151227 | Common:1; Rare:47 | ||||
chr19:42240117-42240247 | Rare:45 | ||||
chr19:42292789-42293082 | Rare:103; Clinvar:3 | ||||
chr19:42387427-42387646 | Rare:73 | ||||
chr19:42396905-42397194 | Common:1; Rare:67 | ||||
chr19:43331494-43331525 | Rare:4 | ||||
chr19:43608022-43608272 | Common:1; Rare:63 | ||||
chr19:43668920-43669004 | Common:1; Rare:18 | ||||
chr19:44245492-44245726 | Rare:38 | ||||
chr19:44275653-44275758 | Rare:23 | ||||
chr19:44803386-44803639 | Common:2; Rare:44 | ||||
chr19:44874975-44875259 | Common:1; Rare:45 |