Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:28581869-28582028 | Common:1; Rare:46 | ||||
chr1:28648302-28648605 | Common:4; Rare:87 | ||||
chr1:30824123-30824292 | Common:1; Rare:24 | ||||
chr1:30936811-30936923 | Common:1; Rare:22 | ||||
chr1:31348709-31348874 | Common:1; Rare:32 | ||||
chr1:31580528-31580823 | Rare:73 | ||||
chr1:31679797-31679925 | Rare:46 | ||||
chr1:31701584-31701664 | Rare:15 | ||||
chr1:32232156-32232470 | Common:2; Rare:64 | ||||
chr1:35831516-35831842 | Rare:58 | ||||
chr1:39632952-39633241 | Rare:71 | ||||
chr1:42929761-42929929 | Common:1; Rare:43; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
chr1:58576068-58576169 | Common:2; Rare:19; Clinvar:2; Clinvar (benign):2 | ||||
chr1:58783054-58783145 | Common:2; Rare:27 | ||||
chr1:58783157-58783257 | Rare:25 |