Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99732072-99732331 | Rare:95; Clinvar:4 | ||||
chr10:100185938-100186165 | Rare:85 | ||||
chr10:100346921-100347290 | Common:1; Rare:88 | ||||
chr10:100529836-100530017 | Common:1; Rare:47 | ||||
chr10:100913328-100913357 | Rare:10 | ||||
chr10:100987439-100987590 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031117-101031264 | Common:1; Rare:33 | ||||
chr10:101588205-101588329 | Rare:50 | ||||
chr10:101818136-101818196 | Rare:15 | ||||
chr10:101818342-101818778 | Common:1; Rare:118 | ||||
chr10:102056100-102056368 | Common:1; Rare:64 | ||||
chr10:102114903-102115133 | Common:3; Rare:62 | ||||
chr10:102120153-102120453 | Common:2; Rare:83 | ||||
chr10:102245229-102245590 | Common:1; Rare:67 | ||||
chr10:102418741-102419057 | Rare:66 |