Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42846401-42846638 | Common:1; Rare:65 | ||||
chr1:42958834-42959070 | Common:3; Rare:67; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172055-43172402 | Common:3; Rare:139 | ||||
chr1:43358818-43359006 | Rare:46 | ||||
chr1:43367989-43368197 | Rare:54 | ||||
chr1:43389752-43389945 | Common:3; Rare:87 | ||||
chr1:43605429-43605586 | Common:1; Rare:60 | ||||
chr1:43649956-43650182 | Rare:58 | ||||
chr1:43946449-43946987 | Rare:136 | ||||
chr1:43969776-43970018 | Rare:62 | ||||
chr1:43974823-43975130 | Common:4; Rare:82 | ||||
chr1:43979884-43980018 | Common:2; Rare:32 | ||||
chr1:44213348-44213576 | Common:1; Rare:45 | ||||
chr1:44355276-44355449 | Common:1; Rare:42 | ||||
chr1:44674406-44674760 | Common:3; Rare:95 |