Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373373-234373562 | Common:1; Rare:98; Clinvar (benign):4 | ||||
chr1:234373645-234373775 | Rare:49; Clinvar (benign):3 | ||||
chr1:236523884-236524024 | Common:2; Rare:37 | ||||
chr1:236604461-236604645 | Common:4; Rare:56 | ||||
chr1:236795053-236795392 | Common:6; Rare:139; Clinvar:3 | ||||
chr1:241519674-241519977 | Common:2; Rare:95; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr1:241848076-241848255 | Common:2; Rare:38 | ||||
chr1:243255040-243255420 | Common:1; Rare:89 | ||||
chr1:243255783-243256113 | Rare:91; Clinvar:4 | ||||
chr1:244451840-244452185 | Common:1; Rare:121 | ||||
chr1:244835575-244835724 | Common:2; Rare:66; Clinvar (benign):4 | ||||
chr1:244864358-244864686 | Rare:126 | ||||
chr1:246566180-246566576 | Common:1; Rare:132 | ||||
chr10:135346-135540 | Rare:53 | ||||
chr10:988334-988470 | Rare:52 |