Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155701730-155701757 | Rare:3 | ||||
chr1:155726752-155726900 | Common:1; Rare:29 | ||||
chr1:155904454-155904671 | Common:2; Rare:63; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:155946717-155946953 | Rare:39 | ||||
chr1:155965046-155965660 | Common:3; Rare:134 | ||||
chr1:155980130-155980350 | Rare:28 | ||||
chr1:156120993-156121286 | Rare:37 | ||||
chr1:156124929-156125013 | Rare:16 | ||||
chr1:156133696-156134015 | Common:1; Rare:64 | ||||
chr1:156468541-156468578 | Rare:6 | ||||
chr1:156486863-156487068 | Rare:35 | ||||
chr1:156708075-156708368 | Rare:56 | ||||
chr1:156897239-156897386 | Rare:22 | ||||
chr1:156910662-156911016 | Rare:73 | ||||
chr1:157995217-157995515 | Common:2; Rare:46 |