Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236065039-236065274 | Common:2; Rare:97; Clinvar (pathogenic):1 | ||||
chr1:236523660-236524060 | Common:5; Rare:97 | ||||
chr1:240611943-240612251 | Rare:78 | ||||
chr1:241519643-241519977 | Common:3; Rare:107; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
chr1:241848114-241848255 | Common:1; Rare:25 | ||||
chr1:243255047-243255358 | Common:1; Rare:69 | ||||
chr1:243255776-243256140 | Common:1; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451761-244452304 | Common:1; Rare:174 | ||||
chr1:244461371-244461408 | Rare:11 | ||||
chr1:244835562-244835747 | Common:2; Rare:82; Clinvar (benign):5 | ||||
chr1:244863975-244863992 | Rare:2 | ||||
chr1:244864243-244864686 | Rare:162; Clinvar:1 | ||||
chr1:244970251-244970430 | Common:3; Rare:83 | ||||
chr1:246566118-246566584 | Common:2; Rare:158 | ||||
chr1:246724212-246724611 | Common:2; Rare:133 |