Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40450042-40450174 | Common:3; Rare:44 | ||||
chr1:40531497-40531715 | Rare:60 | ||||
chr1:40979394-40979810 | Common:5; Rare:132 | ||||
chr1:42335175-42335335 | Common:1; Rare:82 | ||||
chr1:42456060-42456348 | Common:1; Rare:68 | ||||
chr1:42658295-42658511 | Common:2; Rare:69 | ||||
chr1:42766996-42767303 | Common:4; Rare:102; Clinvar (benign):1 | ||||
chr1:42817268-42817567 | Rare:96 | ||||
chr1:42846392-42846638 | Common:1; Rare:68 | ||||
chr1:43358674-43359096 | Common:7; Rare:129 | ||||
chr1:43367989-43368208 | Rare:59 | ||||
chr1:43389758-43389940 | Common:3; Rare:80 | ||||
chr1:43707337-43707648 | Common:2; Rare:88 | ||||
chr1:43946645-43946954 | Rare:81 | ||||
chr1:44739635-44739939 | Common:3; Rare:123 |