Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4723738-4724067 | Common:6; Rare:126 | ||||
chr19:4831707-4832044 | Common:3; Rare:62 | ||||
chr19:4867626-4867817 | Common:3; Rare:57 | ||||
chr19:5622734-5623141 | Common:5; Rare:151 | ||||
chr19:5978078-5978411 | Common:3; Rare:126 | ||||
chr19:6110523-6110832 | Common:2; Rare:94 | ||||
chr19:7395045-7395164 | Common:2; Rare:36 | ||||
chr19:7489017-7489153 | Common:2; Rare:61 | ||||
chr19:7629528-7629848 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7637007-7637143 | Common:2; Rare:47; Clinvar (benign):1 | ||||
chr19:7943627-7943984 | Rare:99 | ||||
chr19:8321328-8321703 | Common:2; Rare:152 | ||||
chr19:8363959-8364161 | Common:1; Rare:50 | ||||
chr19:8390127-8390411 | Rare:89 | ||||
chr19:9827626-9827954 | Common:2; Rare:89 |