Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209784523-209784705 | Rare:58 | ||||
chr1:209806008-209806269 | Common:4; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827861-209828090 | Common:1; Rare:61 | ||||
chr1:209937970-209938267 | Common:3; Rare:101; Clinvar (pathogenic):1 | ||||
chr1:210232728-210232965 | Common:2; Rare:60 | ||||
chr1:210439236-210439455 | Rare:43 | ||||
chr1:211259745-211259975 | Rare:65 | ||||
chr1:211675589-211675762 | Rare:34 | ||||
chr1:212035507-212035801 | Common:2; Rare:77 | ||||
chr1:212414782-212414969 | Common:3; Rare:66 | ||||
chr1:212608026-212608761 | Common:5; Rare:165 | ||||
chr1:212791750-212791930 | Common:4; Rare:73 | ||||
chr1:212858081-212858248 | Common:3; Rare:37 | ||||
chr1:213015443-213015593 | Rare:40 | ||||
chr1:213015742-213015927 | Rare:51 |