Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44141483-44141636 | Common:2; Rare:21 | ||||
chr19:44304986-44305141 | Rare:43 | ||||
chr19:44777719-44777916 | Rare:59 | ||||
chr19:44955237-44955410 | Common:2; Rare:50 | ||||
chr19:45038955-45039105 | Rare:53 | ||||
chr19:45406341-45406649 | Common:1; Rare:67 | ||||
chr19:45423509-45423813 | Common:3; Rare:64; Clinvar (benign):1 | ||||
chr19:45507227-45507508 | Common:1; Rare:72 | ||||
chr19:45769203-45769425 | Common:1; Rare:84 | ||||
chr19:46346941-46347105 | Common:3; Rare:52 | ||||
chr19:46601019-46601411 | Common:4; Rare:126; Clinvar (benign):1 | ||||
chr19:46608292-46608531 | Common:1; Rare:58; Clinvar (benign):5 | ||||
chr19:46745750-46746061 | Common:4; Rare:64 | ||||
chr19:47256460-47256568 | Rare:39 | ||||
chr19:47484087-47484300 | Common:2; Rare:76; Clinvar:1 |