Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:14622082-14622295 | Common:1; Rare:15 | ||||
chr19:16078553-16078619 | Rare:14 | ||||
chr19:17560186-17560357 | Common:1; Rare:48 | ||||
chr19:18279631-18279794 | Rare:65 | ||||
chr19:18280142-18280328 | Common:2; Rare:70 | ||||
chr19:18520162-18520313 | Rare:27 | ||||
chr19:18788488-18788731 | Rare:67; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:18904775-18905021 | Rare:53 | ||||
chr19:20423687-20423833 | Common:1; Rare:36 | ||||
chr19:27793211-27793475 | Common:4; Rare:62 | ||||
chr19:27793667-27794049 | Common:1; Rare:98 | ||||
chr19:31519366-31519461 | Rare:18 | ||||
chr19:36331725-36331934 | Common:1; Rare:49 | ||||
chr19:38004580-38004814 | Common:3; Rare:51 | ||||
chr19:38683693-38683972 | Common:2; Rare:43 |