Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:84501955-84502019 | Common:1; Rare:26 | ||||
chr1:91734639-91734851 | Common:3; Rare:54 | ||||
chr1:92840268-92840605 | Common:1; Rare:65 | ||||
chr1:93616643-93616922 | Rare:49 | ||||
chr1:93617004-93617155 | Rare:24 | ||||
chr1:93660297-93660554 | Rare:42 | ||||
chr1:94247651-94247868 | Common:2; Rare:72 | ||||
chr1:99662052-99662399 | Common:1; Rare:55 | ||||
chr1:99670249-99670535 | Common:2; Rare:46 | ||||
chr1:99674515-99674736 | Rare:47 | ||||
chr1:100959636-100959758 | Rare:17 | ||||
chr1:107606601-107606943 | Common:3; Rare:37 | ||||
chr1:108898455-108898694 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
chr1:108901603-108901887 | Common:4; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
chr1:108924616-108924878 | Common:2; Rare:35 |