Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:62875315-62875450 | Common:1; Rare:33 | ||||
chr3:63863732-63864150 | Common:7; Rare:138 | ||||
chr3:63912011-63912042 | Rare:7 | ||||
chr3:64225069-64225336 | Common:2; Rare:46; Clinvar:5; Clinvar (benign):1 | ||||
chr3:64225412-64225580 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
chr3:65597088-65597311 | Common:1; Rare:35 | ||||
chr3:65597401-65597490 | Rare:12 | ||||
chr3:65597655-65597743 | Common:1; Rare:33 | ||||
chr3:66038764-66039063 | Common:3; Rare:108 | ||||
chr3:66997997-66998359 | Common:2; Rare:90 | ||||
chr3:67654590-67654682 | Rare:34 | ||||
chr3:69052216-69052466 | Common:6; Rare:90 | ||||
chr3:69080349-69080456 | Rare:44 | ||||
chr3:69084808-69085079 | Common:3; Rare:75 | ||||
chr3:69542563-69542769 | Common:2; Rare:57 |