Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373351-234373588 | Common:1; Rare:119; Clinvar (benign):4 | ||||
chr1:234608200-234608246 | Rare:16 | ||||
chr1:235128801-235129035 | Rare:89 | ||||
chr1:235866865-235867177 | Common:3; Rare:100 | ||||
chr1:236281952-236282242 | Common:6; Rare:84 | ||||
chr1:236523845-236524034 | Common:2; Rare:51 | ||||
chr1:236795086-236795319 | Common:4; Rare:83; Clinvar:1 | ||||
chr1:241848078-241848255 | Common:2; Rare:37 | ||||
chr1:243255047-243255415 | Common:1; Rare:84 | ||||
chr1:243255775-243256104 | Rare:90; Clinvar:4 | ||||
chr1:244451851-244452185 | Common:1; Rare:117 | ||||
chr1:244835595-244835729 | Common:1; Rare:61; Clinvar (benign):4 | ||||
chr1:244864386-244864693 | Rare:119 | ||||
chr1:246507241-246507375 | Common:1; Rare:53 | ||||
chr1:246566185-246566579 | Common:1; Rare:129 |