Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44304996-44305141 | Rare:39 | ||||
chr19:44643801-44643918 | Rare:35 | ||||
chr19:44757415-44757569 | Rare:35 | ||||
chr19:44954397-44954599 | Common:2; Rare:50 | ||||
chr19:44992320-44992638 | Common:3; Rare:99 | ||||
chr19:45038943-45039104 | Rare:57 | ||||
chr19:45406341-45406649 | Common:1; Rare:67 | ||||
chr19:45507228-45507535 | Common:1; Rare:84 | ||||
chr19:45584774-45585174 | Common:5; Rare:135; Clinvar:1; Clinvar (benign):4 | ||||
chr19:45730869-45731084 | Common:1; Rare:50 | ||||
chr19:45769203-45769325 | Rare:35 | ||||
chr19:45772714-45773047 | Common:2; Rare:71; Clinvar (benign):1 | ||||
chr19:46296818-46297062 | Common:4; Rare:89 | ||||
chr19:46298143-46298461 | Common:5; Rare:81 | ||||
chr19:46346941-46347148 | Common:3; Rare:73 |