Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49527846-49528049 | Common:3; Rare:67 | ||||
chr19:49528314-49528349 | Rare:4 | ||||
chr19:49556971-49557148 | Rare:77 | ||||
chr19:49560627-49560940 | Rare:74 | ||||
chr19:49580502-49580681 | Rare:58 | ||||
chr19:49581309-49581461 | Common:1; Rare:30 | ||||
chr19:49640079-49640469 | Common:1; Rare:120 | ||||
chr19:49641888-49642245 | Rare:106 | ||||
chr19:49665116-49665473 | Rare:79 | ||||
chr19:49665478-49666112 | Common:6; Rare:267; Clinvar (pathogenic):1 | ||||
chr19:49672194-49672271 | Common:1; Rare:19 | ||||
chr19:49677155-49677315 | Common:1; Rare:62 | ||||
chr19:49677470-49677746 | Rare:84 | ||||
chr19:49690973-49691286 | Common:2; Rare:69 | ||||
chr19:49712805-49713017 | Common:2; Rare:87; Clinvar:1 |