Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42816981-42817136 | Common:1; Rare:43 | ||||
chr1:42846392-42846638 | Common:1; Rare:68 | ||||
chr1:42958754-42959101 | Common:4; Rare:88; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172214-43172353 | Common:1; Rare:67 | ||||
chr1:43270924-43271020 | Rare:25 | ||||
chr1:43358659-43359063 | Common:7; Rare:132 | ||||
chr1:43367981-43368213 | Rare:63 | ||||
chr1:43389757-43389964 | Common:4; Rare:92 | ||||
chr1:43530765-43530925 | Common:2; Rare:61 | ||||
chr1:43649892-43650186 | Rare:70 | ||||
chr1:43707332-43707592 | Common:2; Rare:79 | ||||
chr1:43933666-43933812 | Rare:35 | ||||
chr1:43946649-43946987 | Rare:91 | ||||
chr1:43974778-43975041 | Common:3; Rare:71 | ||||
chr1:44213318-44213542 | Common:1; Rare:49 |