Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27100360-27100700 | Common:5; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
chr10:27153946-27154000 | Rare:12 | ||||
chr10:27154231-27154532 | Rare:84 | ||||
chr10:27155075-27155483 | Common:7; Rare:150; Clinvar:7; Clinvar (benign):8 | ||||
chr10:27240257-27240429 | Rare:50 | ||||
chr10:27240456-27241180 | Common:5; Rare:183 | ||||
chr10:27241798-27241965 | Common:1; Rare:39 | ||||
chr10:27241976-27242359 | Common:2; Rare:140 | ||||
chr10:27503964-27504374 | Common:1; Rare:162; Clinvar:4; Clinvar (benign):1 | ||||
chr10:27504513-27504716 | Rare:74 | ||||
chr10:28532079-28532102 | Rare:6 | ||||
chr10:28532104-28532892 | Common:7; Rare:264 | ||||
chr10:28532952-28533186 | Rare:94 | ||||
chr10:28533774-28533870 | Common:2; Rare:33 | ||||
chr10:28677211-28677555 | Common:6; Rare:156 |