Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24290058-24290320 | Common:3; Rare:46 | ||||
chr1:25875503-25875634 | Rare:40 | ||||
chr1:26858978-26859228 | Common:1; Rare:40 | ||||
chr1:26863770-26864229 | Common:1; Rare:114 | ||||
chr1:26864442-26864577 | Common:1; Rare:27 | ||||
chr1:28581869-28582029 | Common:1; Rare:46 | ||||
chr1:32760944-32760986 | Rare:5 | ||||
chr1:36386508-36386702 | Rare:28 | ||||
chr1:43603438-43603645 | Rare:53 | ||||
chr1:44780735-44780929 | Rare:35 | ||||
chr1:46037218-46037507 | Common:1; Rare:64 | ||||
chr1:46181443-46181649 | Common:2; Rare:41 | ||||
chr1:46302053-46302164 | Common:1; Rare:35 | ||||
chr1:58575423-58575587 | Common:1; Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
chr1:58575912-58576259 | Common:4; Rare:71; Clinvar:2; Clinvar (benign):5 |