Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:42302308-42302512 | Rare:59 | ||||
chr19:42325434-42325702 | Rare:65 | ||||
chr19:42412368-42412690 | Common:2; Rare:61 | ||||
chr19:42423526-42423814 | Common:4; Rare:95 | ||||
chr19:42442896-42442928 | Rare:6 | ||||
chr19:42528433-42528635 | Common:2; Rare:47 | ||||
chr19:43527163-43527335 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr19:43575477-43575778 | Common:2; Rare:86 | ||||
chr19:43580483-43580655 | Common:3; Rare:26 | ||||
chr19:43595976-43596450 | Common:5; Rare:148 | ||||
chr19:43619308-43619537 | Rare:52 | ||||
chr19:43619563-43619675 | Common:1; Rare:34 | ||||
chr19:43670117-43670363 | Common:2; Rare:64 | ||||
chr19:43754840-43755088 | Common:3; Rare:98 | ||||
chr19:43827192-43827444 | Common:4; Rare:51 |