Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49580528-49580648 | Rare:42 | ||||
chr19:49665739-49665980 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
chr19:49690980-49691142 | Rare:36 | ||||
chr19:49813249-49813338 | Rare:36 | ||||
chr19:49851075-49851167 | Rare:33 | ||||
chr19:49854136-49854468 | Common:2; Rare:93 | ||||
chr19:49854548-49854724 | Common:1; Rare:67 | ||||
chr19:49857526-49857775 | Common:3; Rare:95 | ||||
chr19:49867518-49867692 | Common:3; Rare:50; Clinvar:1 | ||||
chr19:49877278-49877742 | Common:1; Rare:125 | ||||
chr19:49877910-49878172 | Common:2; Rare:86 | ||||
chr19:49929430-49929564 | Common:4; Rare:49 | ||||
chr19:50476243-50476550 | Rare:144 | ||||
chr19:50511129-50511168 | Rare:14 | ||||
chr19:50511169-50511187 | Rare:6 |