Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42817205-42817498 | Rare:100 | ||||
chr1:42846392-42846636 | Common:1; Rare:68 | ||||
chr1:42958747-42959100 | Common:4; Rare:89; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172135-43172352 | Common:3; Rare:91 | ||||
chr1:43358662-43359043 | Common:7; Rare:127 | ||||
chr1:43367923-43368208 | Rare:74 | ||||
chr1:43389757-43389955 | Common:3; Rare:90 | ||||
chr1:43707333-43707626 | Common:2; Rare:87 | ||||
chr1:43933632-43933805 | Rare:42 | ||||
chr1:43946561-43947011 | Rare:128 | ||||
chr1:43974804-43975068 | Common:3; Rare:72 | ||||
chr1:44031358-44031668 | Common:2; Rare:63 | ||||
chr1:44674421-44674744 | Common:3; Rare:83 | ||||
chr1:44739634-44739923 | Common:2; Rare:114 | ||||
chr1:44775462-44775622 | Common:1; Rare:64 |