Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38315907-38316147 | Common:1; Rare:65 | ||||
chr19:38374483-38374805 | Rare:125 | ||||
chr19:38647421-38647737 | Common:3; Rare:113 | ||||
chr19:38831762-38832061 | Common:4; Rare:88; Clinvar (benign):1 | ||||
chr19:38899572-38900018 | Rare:132 | ||||
chr19:38930723-38930992 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39391025-39391418 | Common:1; Rare:158 | ||||
chr19:39406699-39406858 | Rare:58 | ||||
chr19:39846323-39846532 | Common:1; Rare:101 | ||||
chr19:39970986-39971196 | Common:2; Rare:56 | ||||
chr19:39996956-39997101 | Common:4; Rare:50 | ||||
chr19:40056157-40056270 | Rare:16 | ||||
chr19:40090878-40090989 | Common:1; Rare:30 | ||||
chr19:40285240-40285553 | Common:1; Rare:115 | ||||
chr19:40341897-40342084 | Rare:45 |