Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235866849-235867174 | Common:3; Rare:101 | ||||
chr1:236281943-236282116 | Common:3; Rare:50 | ||||
chr1:236523899-236524024 | Common:2; Rare:34 | ||||
chr1:236524512-236524608 | Common:1; Rare:20 | ||||
chr1:236604453-236604628 | Common:4; Rare:55 | ||||
chr1:236795080-236795418 | Common:6; Rare:139; Clinvar:3 | ||||
chr1:241519655-241519977 | Common:2; Rare:105; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
chr1:241848078-241848281 | Common:2; Rare:37 | ||||
chr1:243254387-243254433 | Rare:10 | ||||
chr1:243255040-243255433 | Common:1; Rare:96 | ||||
chr1:243255697-243256157 | Common:1; Rare:131; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451789-244452218 | Common:1; Rare:146 | ||||
chr1:244835193-244835343 | Rare:63 | ||||
chr1:244864243-244864728 | Common:1; Rare:186; Clinvar:1 | ||||
chr1:244970234-244970413 | Common:4; Rare:90 |