Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149887908-149888215 | Rare:93 | ||||
chr1:149927727-149927922 | Common:1; Rare:73; Clinvar (benign):5 | ||||
chr1:150010503-150010651 | Common:2; Rare:29 | ||||
chr1:150067138-150067358 | Common:4; Rare:39 | ||||
chr1:150067606-150067905 | Common:1; Rare:84 | ||||
chr1:150149410-150149691 | Rare:54 | ||||
chr1:150150503-150150865 | Common:5; Rare:102 | ||||
chr1:150235950-150236071 | Rare:29 | ||||
chr1:150272374-150272747 | Common:1; Rare:63 | ||||
chr1:150282158-150282288 | Rare:33 | ||||
chr1:150282299-150282591 | Common:3; Rare:57 | ||||
chr1:150293810-150293913 | Rare:35 | ||||
chr1:150321421-150321597 | Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363968-150364201 | Common:3; Rare:85 | ||||
chr1:150364572-150364775 | Common:1; Rare:74 |