Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4007507-4007758 | Common:3; Rare:102 | ||||
chr19:4182495-4182607 | Rare:39; Clinvar:1 | ||||
chr19:4304526-4304690 | Common:3; Rare:52 | ||||
chr19:4867618-4867820 | Common:3; Rare:63 | ||||
chr19:5622737-5623181 | Common:5; Rare:171 | ||||
chr19:5680482-5680777 | Rare:88 | ||||
chr19:5978075-5978383 | Common:3; Rare:114 | ||||
chr19:6199522-6199855 | Common:11; Rare:106 | ||||
chr19:6740809-6740927 | Rare:26 | ||||
chr19:7489006-7489070 | Rare:30 | ||||
chr19:7629507-7629848 | Common:5; Rare:127; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7920189-7920393 | Rare:83 | ||||
chr19:8321328-8321557 | Common:2; Rare:109 | ||||
chr19:8390044-8390411 | Common:1; Rare:105 | ||||
chr19:8444807-8445040 | Common:2; Rare:106 |