Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4472023-4472297 | Common:2; Rare:95 | ||||
chr19:4639199-4639587 | Common:1; Rare:129 | ||||
chr19:4670057-4670448 | Common:8; Rare:139 | ||||
chr19:4831672-4831913 | Common:3; Rare:59 | ||||
chr19:5293213-5293415 | Common:1; Rare:93 | ||||
chr19:5622765-5623181 | Common:5; Rare:153 | ||||
chr19:5680479-5680771 | Rare:85 | ||||
chr19:5680884-5681055 | Rare:45 | ||||
chr19:5719802-5719943 | Common:1; Rare:60; Clinvar:1 | ||||
chr19:5978066-5978390 | Common:3; Rare:122 | ||||
chr19:7489017-7489071 | Rare:24 | ||||
chr19:7629529-7629848 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7637014-7637149 | Common:2; Rare:46; Clinvar (benign):1 | ||||
chr19:7920149-7920427 | Rare:104 | ||||
chr19:8321308-8321653 | Common:2; Rare:151 |