Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235328116-235328584 | Common:3; Rare:136 | ||||
chr1:236065045-236065395 | Common:4; Rare:127; Clinvar (pathogenic):1 | ||||
chr1:236523894-236524060 | Common:2; Rare:45 | ||||
chr1:236604456-236604593 | Common:4; Rare:44 | ||||
chr1:236795170-236795327 | Common:3; Rare:57; Clinvar:2 | ||||
chr1:241848082-241848223 | Common:1; Rare:30 | ||||
chr1:243255191-243255358 | Common:1; Rare:35 | ||||
chr1:243255773-243256113 | Rare:95; Clinvar:4 | ||||
chr1:244352510-244352640 | Rare:27 | ||||
chr1:244451807-244452090 | Rare:105 | ||||
chr1:244461266-244461325 | Common:1; Rare:14 | ||||
chr1:244835016-244835333 | Rare:118 | ||||
chr1:244835562-244835721 | Common:2; Rare:69; Clinvar (benign):3 | ||||
chr1:244863943-244864128 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):3 | ||||
chr1:244864377-244864669 | Rare:107 |