Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659231-99659556 | Common:1; Rare:84 | ||||
chr10:99732053-99732335 | Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185895-100186198 | Rare:113 | ||||
chr10:100229571-100229704 | Common:1; Rare:45 | ||||
chr10:100267595-100267776 | Common:3; Rare:58 | ||||
chr10:100286609-100286730 | Common:4; Rare:71 | ||||
chr10:100346470-100346668 | Common:3; Rare:43 | ||||
chr10:100346911-100347438 | Common:3; Rare:119 | ||||
chr10:100529831-100530006 | Common:1; Rare:48 | ||||
chr10:100535747-100535961 | Common:6; Rare:78 | ||||
chr10:100912745-100913023 | Common:1; Rare:87 | ||||
chr10:100913328-100913464 | Rare:34 | ||||
chr10:100969222-100969564 | Common:3; Rare:86 | ||||
chr10:100987156-100987611 | Common:2; Rare:161; Clinvar:1; Clinvar (benign):2 | ||||
chr10:100996940-100997095 | Common:1; Rare:43 |