Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234608194-234608573 | Common:2; Rare:153; Clinvar (benign):1 | ||||
chr1:235128791-235129009 | Rare:84 | ||||
chr1:235328127-235328287 | Common:2; Rare:58 | ||||
chr1:236064991-236065415 | Common:4; Rare:142; Clinvar (pathogenic):1 | ||||
chr1:236281936-236282258 | Common:6; Rare:95 | ||||
chr1:236523872-236524024 | Common:2; Rare:39 | ||||
chr1:236540422-236540623 | Common:5; Rare:70 | ||||
chr1:236604462-236604628 | Common:4; Rare:51 | ||||
chr1:243255191-243255358 | Common:1; Rare:35 | ||||
chr1:243255762-243256124 | Rare:102; Clinvar:4 | ||||
chr1:244451813-244452132 | Common:1; Rare:117 | ||||
chr1:244835197-244835333 | Rare:58 | ||||
chr1:244835525-244835736 | Common:3; Rare:94; Clinvar (benign):4 | ||||
chr1:244863943-244864728 | Common:2; Rare:275; Clinvar:3; Clinvar (benign):6 | ||||
chr1:244970074-244970421 | Common:5; Rare:148 |