Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39390850-39390925 | Rare:31 | ||||
chr19:39391025-39391425 | Common:1; Rare:161 | ||||
chr19:39435888-39436132 | Common:4; Rare:94 | ||||
chr19:39480685-39480912 | Common:3; Rare:120; Clinvar (pathogenic):1 | ||||
chr19:39846335-39846479 | Common:1; Rare:66 | ||||
chr19:39970918-39971196 | Common:4; Rare:76 | ||||
chr19:39996915-39997084 | Common:5; Rare:50 | ||||
chr19:40056148-40056277 | Rare:18 | ||||
chr19:40090886-40090990 | Common:1; Rare:28 | ||||
chr19:40285257-40285537 | Common:1; Rare:106 | ||||
chr19:40348388-40348739 | Common:4; Rare:117 | ||||
chr19:40465735-40466104 | Common:3; Rare:107 | ||||
chr19:40715074-40715187 | Rare:30 | ||||
chr19:41262336-41262566 | Rare:44 | ||||
chr19:41860158-41860281 | Rare:45; Clinvar:2 |