Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235328116-235328409 | Common:2; Rare:85 | ||||
chr1:235328813-235328954 | Rare:45 | ||||
chr1:236281950-236282258 | Common:6; Rare:91 | ||||
chr1:236604453-236604645 | Common:4; Rare:59 | ||||
chr1:236795088-236795414 | Common:5; Rare:138; Clinvar:3 | ||||
chr1:241519678-241519963 | Common:2; Rare:92; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr1:241848118-241848251 | Common:1; Rare:24 | ||||
chr1:243255776-243256077 | Rare:82; Clinvar:4 | ||||
chr1:244451813-244452212 | Common:1; Rare:135 | ||||
chr1:244835580-244835723 | Common:2; Rare:64; Clinvar (benign):4 | ||||
chr1:244864421-244864723 | Common:1; Rare:120 | ||||
chr1:244970608-244970846 | Common:6; Rare:61 | ||||
chr1:246566228-246566584 | Common:1; Rare:117 | ||||
chr1:247078703-247078902 | Common:1; Rare:65 | ||||
chr1:247104295-247104531 | Common:2; Rare:73 |