Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99403467-99403870 | Rare:91 | ||||
chr10:99430533-99430986 | Common:4; Rare:118 | ||||
chr10:99659207-99659595 | Common:2; Rare:99 | ||||
chr10:99732053-99732360 | Rare:117; Clinvar:5; Clinvar (benign):1 | ||||
chr10:99782468-99782876 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
chr10:100185710-100186197 | Rare:164 | ||||
chr10:100229547-100229639 | Rare:29 | ||||
chr10:100535856-100535955 | Common:6; Rare:53 | ||||
chr10:100912675-100913023 | Common:1; Rare:102 | ||||
chr10:100987090-100987598 | Common:1; Rare:184; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996986-100997148 | Common:1; Rare:48 | ||||
chr10:101031117-101031279 | Common:1; Rare:36 | ||||
chr10:101588166-101588338 | Rare:72 | ||||
chr10:101818334-101818778 | Common:1; Rare:120 | ||||
chr10:102056089-102056337 | Common:1; Rare:59 |