Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149917812-149918003 | Common:1; Rare:50 | ||||
chr1:149927736-149927997 | Common:2; Rare:100; Clinvar (benign):6 | ||||
chr1:149928223-149928382 | Common:1; Rare:30 | ||||
chr1:150010639-150010978 | Common:2; Rare:89 | ||||
chr1:150066907-150067343 | Common:4; Rare:78 | ||||
chr1:150067606-150067858 | Common:1; Rare:72 | ||||
chr1:150149272-150149570 | Rare:45 | ||||
chr1:150149625-150149919 | Common:2; Rare:109 | ||||
chr1:150150714-150151114 | Common:7; Rare:214 | ||||
chr1:150234667-150234907 | Rare:42 | ||||
chr1:150236085-150236449 | Rare:81 | ||||
chr1:150256793-150257315 | Common:4; Rare:81 | ||||
chr1:150257600-150257970 | Common:1; Rare:83 | ||||
chr1:150268948-150269289 | Rare:81 | ||||
chr1:150272346-150272682 | Common:1; Rare:54 |