Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:54977619-54977685 | Common:1; Rare:14 | ||||
chr2:54977951-54978041 | Common:2; Rare:20 | ||||
chr2:54980310-54980436 | Rare:24 | ||||
chr2:54980680-54980692 | |||||
chr2:54981458-54981634 | Rare:37 | ||||
chr2:54983362-54983513 | Common:1; Rare:27 | ||||
chr2:54983561-54983773 | Common:1; Rare:40 | ||||
chr2:55023543-55023660 | Rare:13 | ||||
chr2:55023816-55023895 | Rare:12 | ||||
chr2:55037596-55037851 | Common:3; Rare:47 | ||||
chr2:55038523-55038817 | Common:1; Rare:56 | ||||
chr2:55870758-55871076 | Common:1; Rare:74; Clinvar (benign):1 | ||||
chr2:55919950-55920138 | Common:1; Rare:27 | ||||
chr2:55923039-55923100 | Rare:13 | ||||
chr2:60516637-60516794 | Rare:31 |