Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1354793-1354993 | Rare:84 | ||||
chr19:1605408-1605665 | Common:3; Rare:101 | ||||
chr19:2328550-2328693 | Rare:67 | ||||
chr19:2475954-2476132 | Common:1; Rare:55 | ||||
chr19:2783250-2783448 | Rare:71 | ||||
chr19:2785239-2785554 | Common:5; Rare:96 | ||||
chr19:2841179-2841520 | Common:2; Rare:105 | ||||
chr19:2944916-2945196 | Common:5; Rare:96 | ||||
chr19:3985384-3985617 | Common:1; Rare:136 | ||||
chr19:4723755-4724066 | Common:6; Rare:118 | ||||
chr19:5622737-5623185 | Common:5; Rare:175 | ||||
chr19:5680482-5680630 | Rare:43 | ||||
chr19:5978085-5978408 | Common:3; Rare:122 | ||||
chr19:6361772-6361801 | Rare:13 | ||||
chr19:7629532-7629838 | Common:5; Rare:108; Clinvar (benign):2; Clinvar (pathogenic):1 |