Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48398692-48399111 | Rare:151 | ||||
chr19:48714014-48715350 | Common:11; Rare:461; Clinvar:1 | ||||
chr19:48757780-48758140 | Common:2; Rare:122 | ||||
chr19:48780686-48781151 | Common:3; Rare:142 | ||||
chr19:48962424-48962558 | Common:1; Rare:33 | ||||
chr19:48963280-48963810 | Common:6; Rare:160 | ||||
chr19:48963834-48964012 | Common:1; Rare:32 | ||||
chr19:49941466-49941866 | Common:3; Rare:82 | ||||
chr19:49955914-49956346 | Common:3; Rare:153 | ||||
chr19:51354149-51354475 | Common:6; Rare:220; Clinvar:2; Clinvar (benign):10 | ||||
chr19:51354744-51355125 | Common:2; Rare:132 | ||||
chr19:51362720-51363230 | Common:9; Rare:126 | ||||
chr19:51365550-51365800 | Common:6; Rare:84 | ||||
chr19:52601169-52601317 | Common:3; Rare:49 | ||||
chr19:53864360-53864790 | Common:2; Rare:142 |