Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70221278-70221619 | Rare:134 | ||||
chr1:70354654-70354859 | Rare:69 | ||||
chr1:70410958-70411286 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080966-71081437 | Common:1; Rare:133 | ||||
chr1:74198055-74198378 | Common:3; Rare:154 | ||||
chr1:74732998-74733348 | Common:6; Rare:125 | ||||
chr1:74733392-74733508 | Rare:44 | ||||
chr1:75724254-75724449 | Common:4; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
chr1:75724628-75724793 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):2 | ||||
chr1:75786042-75786314 | Common:4; Rare:116 | ||||
chr1:75786464-75786779 | Common:6; Rare:70 | ||||
chr1:76074537-76074754 | Common:2; Rare:88 | ||||
chr1:77219344-77219549 | Common:1; Rare:94 | ||||
chr1:77682580-77682756 | Rare:42 | ||||
chr1:77682905-77683260 | Common:3; Rare:74 |