Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:239386545-239386623 | Rare:11 | ||||
chr1:240612110-240612274 | Rare:33 | ||||
chr1:241519661-241519946 | Common:2; Rare:98; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr1:241848078-241848265 | Common:2; Rare:37 | ||||
chr1:243255040-243255426 | Common:1; Rare:92 | ||||
chr1:243255776-243256113 | Rare:94; Clinvar:4 | ||||
chr1:243487664-243487846 | Common:3; Rare:50 | ||||
chr1:244451778-244452078 | Rare:104 | ||||
chr1:244835091-244835333 | Rare:92 | ||||
chr1:244835583-244835747 | Common:1; Rare:75; Clinvar (benign):5 | ||||
chr1:244863975-244864226 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):5 | ||||
chr1:244864264-244864691 | Rare:161 | ||||
chr1:244969547-244969788 | Rare:64 | ||||
chr1:244970251-244970421 | Common:3; Rare:77 | ||||
chr1:246566170-246566563 | Common:1; Rare:132 |