Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10231252-10231597 | Common:2; Rare:69 | ||||
chr19:10333516-10333738 | Rare:73 | ||||
chr19:10380478-10380824 | Common:12; Rare:102; Clinvar:5 | ||||
chr19:10836275-10836542 | Common:2; Rare:67 | ||||
chr19:11089138-11089533 | Rare:64; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:11197504-11197622 | Common:1; Rare:32 | ||||
chr19:11262473-11262553 | Rare:26 | ||||
chr19:11559198-11559401 | Common:1; Rare:61 | ||||
chr19:11924977-11925149 | Common:5; Rare:51 | ||||
chr19:12551392-12551556 | Common:1; Rare:56 | ||||
chr19:12610694-12610989 | Rare:96 | ||||
chr19:12666689-12666864 | Rare:72; Clinvar:4 | ||||
chr19:12681821-12681960 | Common:2; Rare:63 | ||||
chr19:12722252-12722406 | Rare:30 | ||||
chr19:12722495-12722843 | Common:4; Rare:67 |