Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:3593953-3594176 | Common:3; Rare:37 | ||||
chr18:5238006-5238135 | Common:1; Rare:51 | ||||
chr18:21831384-21831711 | Common:1; Rare:62 | ||||
chr18:60446969-60447302 | Common:1; Rare:65 | ||||
chr19:3977237-3977526 | Common:4; Rare:92; Clinvar (benign):4 | ||||
chr19:4280258-4280358 | Rare:38 | ||||
chr19:27793669-27794024 | Rare:93 | ||||
chr19:31390759-31391035 | Common:3; Rare:57 | ||||
chr19:34393832-34393958 | Common:2; Rare:42 | ||||
chr19:36331740-36331946 | Common:1; Rare:48 | ||||
chr19:38434581-38434746 | Common:1; Rare:24 | ||||
chr19:41500631-41500767 | Common:1; Rare:24 | ||||
chr19:42396905-42397184 | Common:1; Rare:66 | ||||
chr19:45306219-45306448 | Rare:47 | ||||
chr19:46860829-46861126 | Common:3; Rare:95 |