Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48872189-48872455 | Common:2; Rare:89 | ||||
chr19:48993207-48993579 | Common:4; Rare:161; Clinvar:3; Clinvar (benign):3 | ||||
chr19:49157503-49157827 | Common:2; Rare:88; Clinvar:1 | ||||
chr19:49361515-49361696 | Rare:36 | ||||
chr19:49453092-49453311 | Common:1; Rare:70 | ||||
chr19:49527948-49528375 | Common:3; Rare:81 | ||||
chr19:49580533-49580629 | Rare:34 | ||||
chr19:49640192-49640498 | Rare:87 | ||||
chr19:49665725-49666030 | Common:3; Rare:142; Clinvar (pathogenic):1 | ||||
chr19:49690980-49691150 | Common:2; Rare:39 | ||||
chr19:49851042-49851167 | Rare:49 | ||||
chr19:49877220-49877720 | Common:2; Rare:122 | ||||
chr19:49877836-49878179 | Common:5; Rare:110 | ||||
chr19:49929107-49929212 | Common:3; Rare:35 | ||||
chr19:49929404-49929687 | Common:4; Rare:94 |