Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16352440-16352611 | Common:3; Rare:93 | ||||
chr1:19210254-19210395 | Rare:53 | ||||
chr1:19251512-19251833 | Common:6; Rare:104 | ||||
chr1:19596709-19597064 | Common:3; Rare:121 | ||||
chr1:20661352-20661682 | Common:3; Rare:119; Clinvar:4; Clinvar (benign):6 | ||||
chr1:22052533-22052742 | Common:2; Rare:69 | ||||
chr1:23559487-23559677 | Common:2; Rare:79 | ||||
chr1:23959654-23959849 | Common:2; Rare:45 | ||||
chr1:23980269-23980514 | Rare:77 | ||||
chr1:25232454-25232613 | Rare:65 | ||||
chr1:25247449-25247638 | Common:2; Rare:68 | ||||
chr1:25819902-25820013 | Common:1; Rare:34 | ||||
chr1:25859362-25859556 | Common:3; Rare:81 | ||||
chr1:26279948-26280150 | Rare:116 | ||||
chr1:26432258-26432403 | Common:2; Rare:38; Clinvar:2; Clinvar (benign):1 |