Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19210064-19210524 | Common:1; Rare:151 | ||||
chr1:19251505-19251857 | Common:6; Rare:117 | ||||
chr1:19312013-19312333 | Common:8; Rare:153 | ||||
chr1:19485446-19485762 | Rare:118 | ||||
chr1:19799872-19800176 | Common:4; Rare:87 | ||||
chr1:20486217-20486363 | Rare:32 | ||||
chr1:20652629-20652936 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
chr1:20661422-20661727 | Common:1; Rare:109; Clinvar:3; Clinvar (benign):4 | ||||
chr1:20786626-20786837 | Rare:81 | ||||
chr1:21783086-21783260 | Common:2; Rare:60 | ||||
chr1:21839040-21839416 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
chr1:22636519-22636736 | Common:1; Rare:46 | ||||
chr1:23559126-23559246 | Common:1; Rare:50 | ||||
chr1:23559248-23559295 | Rare:22 | ||||
chr1:23559298-23559648 | Common:1; Rare:155 |