Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:893158-893484 | Common:3; Rare:139 | ||||
chr19:1132191-1132480 | Common:1; Rare:112 | ||||
chr19:1155138-1155320 | Rare:57 | ||||
chr19:1354793-1354999 | Rare:86 | ||||
chr19:1438237-1438428 | Common:1; Rare:69 | ||||
chr19:2328562-2328703 | Common:2; Rare:70 | ||||
chr19:3982805-3983291 | Common:5; Rare:174; Clinvar:1; Clinvar (benign):6 | ||||
chr19:4182549-4182591 | Rare:12 | ||||
chr19:5622725-5623181 | Common:5; Rare:177 | ||||
chr19:5978085-5978393 | Common:3; Rare:115 | ||||
chr19:6110471-6110790 | Common:2; Rare:94 | ||||
chr19:6361738-6361867 | Rare:59; Clinvar:1 | ||||
chr19:7395022-7395185 | Common:4; Rare:50 | ||||
chr19:7629528-7629854 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7943694-7943988 | Rare:67 |