Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67430317-67430584 | Rare:105 | ||||
chr1:67833343-67833531 | Common:2; Rare:73 | ||||
chr1:68232429-68232654 | Common:1; Rare:52 | ||||
chr1:70205527-70205778 | Rare:85 | ||||
chr1:70221321-70221540 | Rare:93 | ||||
chr1:70246704-70246907 | Rare:44 | ||||
chr1:70249844-70250013 | Rare:47 | ||||
chr1:70354674-70354862 | Rare:65 | ||||
chr1:70411069-70411276 | Common:1; Rare:51; Clinvar:1 | ||||
chr1:71080948-71081370 | Rare:112 | ||||
chr1:74198148-74198351 | Common:2; Rare:113 | ||||
chr1:74732994-74733367 | Common:6; Rare:131 | ||||
chr1:75724582-75724815 | Common:2; Rare:109; Clinvar:5; Clinvar (benign):2 | ||||
chr1:75732708-75732854 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
chr1:75786784-75787105 | Common:2; Rare:71 |