Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48988406-48988657 | Common:2; Rare:49 | ||||
chr19:49050528-49050652 | Common:2; Rare:51 | ||||
chr19:49098430-49098716 | Rare:71 | ||||
chr19:49104019-49104237 | Rare:61 | ||||
chr19:49491381-49491726 | Common:12; Rare:130 | ||||
chr19:49492291-49492389 | Rare:30 | ||||
chr19:49805897-49806131 | Rare:80 | ||||
chr19:49820226-49820277 | Rare:12 | ||||
chr19:49829837-49830147 | Common:1; Rare:112; Clinvar:5; Clinvar (benign):5 | ||||
chr19:49832011-49832316 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
chr19:49977455-49977569 | Common:3; Rare:25 | ||||
chr19:50661167-50661305 | Common:2; Rare:24 | ||||
chr19:51693466-51694017 | Common:6; Rare:125 | ||||
chr19:51695983-51696083 | Common:1; Rare:15 | ||||
chr19:52094746-52094903 | Common:2; Rare:32 |