Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42681950-42682426 | Common:2; Rare:146 | ||||
chr1:42683047-42683167 | Rare:60 | ||||
chr1:42766961-42767306 | Common:4; Rare:118; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42816961-42817169 | Common:1; Rare:65 | ||||
chr1:42846377-42846701 | Common:1; Rare:100 | ||||
chr1:42943221-42943455 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:42958826-42959193 | Common:5; Rare:97; Clinvar:8; Clinvar (benign):5 | ||||
chr1:43172245-43172390 | Common:1; Rare:73 | ||||
chr1:43270509-43270629 | Rare:22 | ||||
chr1:43270907-43271058 | Rare:35 | ||||
chr1:43285563-43285753 | Common:4; Rare:34 | ||||
chr1:43358638-43359009 | Common:7; Rare:118 | ||||
chr1:43366301-43366660 | Common:3; Rare:67 | ||||
chr1:43367580-43367814 | Common:2; Rare:42 | ||||
chr1:43367971-43368404 | Rare:113 |