Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231528517-231528752 | Common:2; Rare:83 | ||||
chr1:232805190-232805439 | Common:4; Rare:135 | ||||
chr1:232950407-232950690 | Common:4; Rare:102 | ||||
chr1:234373354-234373578 | Common:1; Rare:111; Clinvar (benign):4 | ||||
chr1:235128690-235128730 | Rare:15 | ||||
chr1:235128767-235128851 | Rare:42 | ||||
chr1:235328121-235328579 | Common:3; Rare:131 | ||||
chr1:236065083-236065280 | Common:2; Rare:83 | ||||
chr1:236281952-236282249 | Common:6; Rare:87 | ||||
chr1:236604413-236604651 | Common:4; Rare:72 | ||||
chr1:236794983-236795453 | Common:6; Rare:177; Clinvar:3 | ||||
chr1:239628956-239629151 | Rare:33 | ||||
chr1:241519660-241519977 | Common:2; Rare:102; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr1:241848075-241848280 | Common:2; Rare:38 | ||||
chr1:243255176-243255351 | Common:1; Rare:34 |