Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15834913-15835169 | Common:1; Rare:109 | ||||
chr1:15835805-15836120 | Common:6; Rare:149 | ||||
chr1:16499251-16499368 | Rare:56 | ||||
chr1:16644646-16644782 | Common:1; Rare:2 | ||||
chr1:16913896-16914100 | Common:8; Rare:41 | ||||
chr1:20029481-20029500 | Rare:3 | ||||
chr1:21876028-21876268 | Rare:59; Clinvar:2 | ||||
chr1:21884765-21885447 | Common:3; Rare:211; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:21887215-21887675 | Common:3; Rare:176; Clinvar:13; Clinvar (benign):3 | ||||
chr1:22025188-22025532 | Common:7; Rare:88 | ||||
chr1:27391581-27391821 | Rare:37 | ||||
chr1:28648302-28648618 | Common:4; Rare:102 | ||||
chr1:46718339-46718521 | Common:1; Rare:40 | ||||
chr1:56439831-56439869 | Common:1; Rare:9 | ||||
chr1:56577739-56577973 | Common:3; Rare:39 |