Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212414813-212415009 | Common:6; Rare:114 | ||||
chr1:212432773-212432949 | Rare:101 | ||||
chr1:212608448-212608764 | Common:2; Rare:158 | ||||
chr1:212791649-212791946 | Common:11; Rare:253 | ||||
chr1:212858055-212858468 | Common:10; Rare:181; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:213015423-213015632 | Rare:88 | ||||
chr1:213015716-213015917 | Rare:89 | ||||
chr1:213051177-213051418 | Common:2; Rare:157 | ||||
chr1:213987626-213988114 | Rare:195 | ||||
chr1:213988080-213988480 | Common:5; Rare:137 | ||||
chr1:213988500-213988790 | Common:2; Rare:87 | ||||
chr1:213989425-213989760 | Common:4; Rare:122 | ||||
chr1:214280995-214281350 | Common:4; Rare:270 | ||||
chr1:214281350-214281750 | Common:4; Rare:160 | ||||
chr1:214551553-214551912 | Common:4; Rare:231 |