Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19311990-19312346 | Common:8; Rare:166 | ||||
chr1:19485435-19485794 | Common:1; Rare:136 | ||||
chr1:19596828-19597105 | Common:2; Rare:115 | ||||
chr1:20028143-20028557 | Common:2; Rare:99 | ||||
chr1:20508063-20508205 | Common:2; Rare:52 | ||||
chr1:20661331-20661709 | Common:3; Rare:138; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786636-20786869 | Rare:90 | ||||
chr1:20787219-20787437 | Rare:103 | ||||
chr1:21176878-21177046 | Rare:37 | ||||
chr1:21345467-21345709 | Common:3; Rare:89 | ||||
chr1:21509142-21509428 | Rare:77 | ||||
chr1:21783086-21783272 | Common:2; Rare:66 | ||||
chr1:22451644-22451890 | Common:1; Rare:76 | ||||
chr1:23344234-23344532 | Common:2; Rare:95 | ||||
chr1:23368854-23369262 | Common:3; Rare:115 |