Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:9818809-9818849 | Rare:12 | ||||
chr19:9827778-9827957 | Common:1; Rare:64 | ||||
chr19:10315738-10316028 | Common:6; Rare:131; Clinvar (benign):10 | ||||
chr19:10333491-10333715 | Rare:79 | ||||
chr19:10653839-10653879 | Rare:16 | ||||
chr19:10836200-10836338 | Common:1; Rare:41 | ||||
chr19:10928533-10928795 | Common:1; Rare:72 | ||||
chr19:10960737-10961141 | Common:2; Rare:149; Clinvar (benign):1 | ||||
chr19:11089292-11089533 | Rare:44; Clinvar:10; Clinvar (pathogenic):1 | ||||
chr19:11197508-11197622 | Common:1; Rare:31 | ||||
chr19:11374642-11374733 | Common:1; Rare:31 | ||||
chr19:11419294-11419451 | Rare:30 | ||||
chr19:11559195-11559336 | Common:1; Rare:51 | ||||
chr19:11738837-11739252 | Common:4; Rare:113 | ||||
chr19:11924795-11925127 | Common:6; Rare:75 |