Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4896350-4896580 | Common:15; Rare:65 | ||||
chr19:5171540-5172065 | Common:2; Rare:193 | ||||
chr19:5229496-5230101 | Common:4; Rare:216 | ||||
chr19:5567939-5568128 | Common:4; Rare:124 | ||||
chr19:6576941-6577196 | Common:4; Rare:82 | ||||
chr19:6577460-6577760 | Rare:81 | ||||
chr19:6601735-6601901 | Common:4; Rare:71 | ||||
chr19:6712280-6712580 | Rare:150; Clinvar:2; Clinvar (benign):4 | ||||
chr19:6717749-6717907 | Common:2; Rare:30 | ||||
chr19:6742815-6743040 | Common:1; Rare:58 | ||||
chr19:6744010-6744240 | Common:2; Rare:57 | ||||
chr19:7098650-7099370 | Common:8; Rare:291 | ||||
chr19:7099480-7099780 | Rare:132 | ||||
chr19:7198010-7198400 | Common:12; Rare:211 | ||||
chr19:7460410-7460750 | Common:10; Rare:105 |