Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70230546-70230778 | Rare:42 | ||||
chr1:70230945-70231364 | Rare:55 | ||||
chr1:70231605-70231933 | Rare:57 | ||||
chr1:70231965-70232375 | Rare:87 | ||||
chr1:70246786-70247085 | Rare:63 | ||||
chr1:70277080-70277162 | Rare:13 | ||||
chr1:70354397-70354560 | Rare:51 | ||||
chr1:70354633-70354846 | Rare:71 | ||||
chr1:71067633-71067843 | Common:1; Rare:55 | ||||
chr1:71080937-71081373 | Rare:113 | ||||
chr1:74198126-74198351 | Common:3; Rare:120 | ||||
chr1:74732823-74733355 | Common:6; Rare:169 | ||||
chr1:75724628-75724817 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):2 | ||||
chr1:75786677-75787110 | Common:3; Rare:96 | ||||
chr1:75787347-75787411 | Common:1; Rare:11 |