Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154976024-154976275 | Common:2; Rare:35 | ||||
chr1:154983094-154983418 | Common:2; Rare:67; Clinvar (benign):2 | ||||
chr1:154993845-154994022 | Rare:33 | ||||
chr1:155002075-155002300 | Common:1; Rare:67 | ||||
chr1:155002478-155002957 | Common:2; Rare:75 | ||||
chr1:155003018-155003245 | Common:1; Rare:43 | ||||
chr1:155003277-155003688 | Common:4; Rare:84 | ||||
chr1:155050510-155050776 | Rare:84 | ||||
chr1:155051096-155051479 | Common:2; Rare:125 | ||||
chr1:155051794-155052065 | Common:2; Rare:45 | ||||
chr1:155063601-155063816 | Rare:66 | ||||
chr1:155063844-155063993 | Rare:47 | ||||
chr1:155078765-155078913 | Rare:50 | ||||
chr1:155084750-155085039 | Common:4; Rare:62 | ||||
chr1:155085089-155085570 | Common:4; Rare:142 |