Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:6110523-6110834 | Common:2; Rare:95 | ||||
chr19:6464279-6464304 | Rare:5 | ||||
chr19:7395022-7395185 | Common:4; Rare:50 | ||||
chr19:7489006-7489123 | Rare:53 | ||||
chr19:7629535-7629848 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7636989-7637143 | Common:2; Rare:51; Clinvar (benign):1 | ||||
chr19:7943644-7943970 | Rare:81 | ||||
chr19:8308328-8308638 | Common:2; Rare:89 | ||||
chr19:8321328-8321688 | Common:2; Rare:150 | ||||
chr19:8364007-8364159 | Common:1; Rare:39 | ||||
chr19:8390044-8390412 | Common:1; Rare:105 | ||||
chr19:8444832-8445047 | Common:2; Rare:100 | ||||
chr19:9435559-9435602 | Rare:15 | ||||
chr19:9538574-9538716 | Common:1; Rare:39 | ||||
chr19:9621181-9621548 | Common:3; Rare:103 |