Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35268591-35269125 | Common:4; Rare:110 | ||||
chr19:35498872-35498978 | Rare:26 | ||||
chr19:35503114-35503359 | Common:2; Rare:47 | ||||
chr19:35505717-35505952 | Common:1; Rare:70 | ||||
chr19:35510293-35510610 | Rare:72 | ||||
chr19:35545438-35545797 | Common:4; Rare:116 | ||||
chr19:35557864-35557982 | Common:1; Rare:33 | ||||
chr19:35612642-35612848 | Common:1; Rare:67 | ||||
chr19:35628801-35629217 | Common:5; Rare:117 | ||||
chr19:35648110-35648402 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr19:35736972-35737250 | Rare:71 | ||||
chr19:35740385-35740808 | Common:6; Rare:158 | ||||
chr19:35745346-35745715 | Rare:110 | ||||
chr19:35748286-35748699 | Common:3; Rare:120 | ||||
chr19:35757935-35758205 | Common:2; Rare:80 |