Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243186289-243186869 | Rare:111 | ||||
chr1:243255040-243255440 | Common:1; Rare:98 | ||||
chr1:243255755-243256135 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244048224-244048551 | Rare:104 | ||||
chr1:244451813-244452309 | Common:2; Rare:157 | ||||
chr1:244834954-244835044 | Rare:20 | ||||
chr1:244835192-244835333 | Rare:59 | ||||
chr1:244835561-244835752 | Common:2; Rare:85; Clinvar (benign):5 | ||||
chr1:244864005-244864260 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):5 | ||||
chr1:244864264-244864728 | Common:1; Rare:181 | ||||
chr1:244970066-244970413 | Common:5; Rare:152 | ||||
chr1:244970601-244970844 | Common:6; Rare:64 | ||||
chr1:246507204-246507375 | Common:1; Rare:68 | ||||
chr1:246566140-246566607 | Common:3; Rare:156 | ||||
chr1:248825848-248825977 | Common:2; Rare:32 |