Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21876370-21876613 | Common:1; Rare:83; Clinvar:6; Clinvar (benign):1 | ||||
chr1:21880476-21880745 | Common:3; Rare:88; Clinvar:5; Clinvar (benign):3 | ||||
chr1:21884818-21885157 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:21890024-21890411 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
chr1:21907836-21908057 | Common:1; Rare:31 | ||||
chr1:23369959-23369963 | |||||
chr1:23755772-23755880 | Common:4; Rare:32 | ||||
chr1:26942653-26943002 | Rare:117 | ||||
chr1:28581855-28582167 | Common:2; Rare:91 | ||||
chr1:28648330-28648613 | Common:4; Rare:93 | ||||
chr1:30824141-30824275 | Common:1; Rare:20 | ||||
chr1:31580522-31580629 | Rare:30 | ||||
chr1:33346917-33347252 | Common:1; Rare:64 | ||||
chr1:35807536-35807652 | Rare:20 | ||||
chr1:36386529-36386703 | Rare:24 |