Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26279871-26280158 | Rare:159 | ||||
chr1:26432112-26432422 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472137-26472437 | Common:5; Rare:86 | ||||
chr1:26472541-26472619 | Rare:34 | ||||
chr1:26695850-26696058 | Rare:68 | ||||
chr1:26787669-26788227 | Common:3; Rare:168; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890241-26890347 | Common:1; Rare:42 | ||||
chr1:26921529-26921800 | Common:3; Rare:80 | ||||
chr1:27366911-27367030 | Rare:23 | ||||
chr1:28088565-28088807 | Common:3; Rare:82 | ||||
chr1:28505881-28506050 | Common:1; Rare:74 | ||||
chr1:28552871-28553125 | Common:2; Rare:98 | ||||
chr1:28643020-28643200 | Rare:69 | ||||
chr1:28736668-28737029 | Common:2; Rare:119 | ||||
chr1:28914326-28914595 | Rare:85 |