Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40979394-40979755 | Common:5; Rare:115 | ||||
chr1:42335175-42335264 | Common:1; Rare:39 | ||||
chr1:42456010-42456103 | Rare:31 | ||||
chr1:42682608-42682731 | Common:1; Rare:50 | ||||
chr1:42766996-42767311 | Common:4; Rare:105; Clinvar (benign):1 | ||||
chr1:42817004-42817139 | Common:1; Rare:35 | ||||
chr1:42846392-42846646 | Common:1; Rare:71 | ||||
chr1:42958821-42959046 | Common:3; Rare:62; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172185-43172334 | Common:1; Rare:64 | ||||
chr1:43358818-43359006 | Rare:46 | ||||
chr1:43367946-43368190 | Rare:61 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 | ||||
chr1:43946649-43946983 | Rare:89 | ||||
chr1:43974788-43975058 | Common:3; Rare:73 | ||||
chr1:44674421-44674773 | Common:3; Rare:91 |