Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:18557663-18557892 | Common:5; Rare:60 | ||||
chr19:18571520-18571906 | Common:6; Rare:137 | ||||
chr19:18683451-18683688 | Common:2; Rare:67 | ||||
chr19:18919344-18919703 | Common:2; Rare:114 | ||||
chr19:19033488-19033658 | Common:1; Rare:52 | ||||
chr19:19192124-19192254 | Common:1; Rare:39 | ||||
chr19:19320490-19320829 | Common:4; Rare:113 | ||||
chr19:19516157-19516295 | Rare:86; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr19:19628190-19628289 | Rare:25 | ||||
chr19:24087013-24087184 | Rare:30 | ||||
chr19:29606172-29606315 | Rare:48 | ||||
chr19:32971939-32972266 | Common:4; Rare:91 | ||||
chr19:33521765-33521956 | Common:1; Rare:57; Clinvar:3 | ||||
chr19:34172329-34172536 | Rare:90 | ||||
chr19:35545482-35545689 | Common:4; Rare:69 |