Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:2721319-2721502 | Common:1; Rare:48 | ||||
chr19:2739955-2740204 | Rare:87 | ||||
chr19:2783209-2783514 | Rare:105 | ||||
chr19:2785233-2785573 | Common:5; Rare:106 | ||||
chr19:2841187-2841557 | Common:2; Rare:118 | ||||
chr19:2944899-2945224 | Common:6; Rare:111 | ||||
chr19:3270397-3270640 | Common:1; Rare:64 | ||||
chr19:3435180-3435416 | Common:1; Rare:79 | ||||
chr19:3500658-3500695 | Rare:13 | ||||
chr19:3500928-3500977 | Rare:12 | ||||
chr19:3880432-3880990 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
chr19:3971023-3971394 | Common:2; Rare:135 | ||||
chr19:3982805-3983194 | Common:5; Rare:139; Clinvar:1; Clinvar (benign):3 | ||||
chr19:3985378-3985651 | Common:1; Rare:154 | ||||
chr19:4007427-4007763 | Common:3; Rare:124 |