Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48993296-48993575 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
chr19:49085100-49085492 | Common:3; Rare:153 | ||||
chr19:49487258-49487675 | Common:5; Rare:157 | ||||
chr19:49527675-49528031 | Common:4; Rare:100 | ||||
chr19:49580536-49580681 | Rare:45 | ||||
chr19:49665813-49666034 | Common:2; Rare:116; Clinvar (pathogenic):1 | ||||
chr19:49867518-49867687 | Common:3; Rare:47; Clinvar:1 | ||||
chr19:49877448-49877706 | Common:1; Rare:67 | ||||
chr19:49877839-49878141 | Common:4; Rare:94 | ||||
chr19:49929923-49930219 | Common:1; Rare:70 | ||||
chr19:50476230-50476542 | Common:1; Rare:145 | ||||
chr19:50723185-50723377 | Common:2; Rare:48 | ||||
chr19:52028360-52028453 | Common:2; Rare:17 | ||||
chr19:52139901-52140126 | Common:1; Rare:63 | ||||
chr19:52269422-52269608 | Common:1; Rare:64 |