Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207051202-207051540 | Rare:82 | ||||
chr1:207052906-207053374 | Common:3; Rare:222 | ||||
chr1:207088200-207089471 | Common:11; Rare:342 | ||||
chr1:207320963-207321211 | Common:4; Rare:73 | ||||
chr1:207321265-207321872 | Common:6; Rare:295 | ||||
chr1:207321895-207322190 | Common:2; Rare:114 | ||||
chr1:207322182-207322640 | Common:1; Rare:249; Clinvar:2 | ||||
chr1:207751715-207752307 | Common:5; Rare:324; Clinvar:2 | ||||
chr1:207752317-207752495 | Rare:33 | ||||
chr1:208244231-208244535 | Common:1; Rare:88 | ||||
chr1:209651115-209651441 | Common:4; Rare:84 | ||||
chr1:209652366-209652609 | Common:4; Rare:102; Clinvar:4; Clinvar (benign):2 | ||||
chr1:209784525-209784755 | Common:2; Rare:144 | ||||
chr1:209827838-209828074 | Common:2; Rare:113 | ||||
chr1:210328720-210328990 | Common:1; Rare:96 |