Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212792240-212792460 | Common:3; Rare:37 | ||||
chr1:212792469-212792525 | Common:2; Rare:19 | ||||
chr1:212857746-212857966 | Common:1; Rare:40 | ||||
chr1:212858021-212858560 | Common:6; Rare:156; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:212858585-212858678 | Common:2; Rare:40; Clinvar (benign):1 | ||||
chr1:212858750-212859013 | Rare:81; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:212859015-212859036 | Rare:7; Clinvar (pathogenic):1 | ||||
chr1:212859164-212859428 | Common:1; Rare:57; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:212950385-212950609 | Common:2; Rare:56 | ||||
chr1:213015171-213015950 | Rare:216 | ||||
chr1:213050943-213050977 | Common:1; Rare:6 | ||||
chr1:213051016-213051557 | Common:4; Rare:170 | ||||
chr1:213051627-213051803 | Rare:35 | ||||
chr1:213987858-213988040 | Rare:39 | ||||
chr1:213988289-213988452 | Common:3; Rare:46 |