Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19596869-19597080 | Common:2; Rare:101 | ||||
chr1:19799858-19800025 | Common:3; Rare:61 | ||||
chr1:20185938-20186128 | Common:1; Rare:63 | ||||
chr1:20661331-20661687 | Common:3; Rare:130; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786617-20786877 | Rare:100 | ||||
chr1:21176883-21177039 | Rare:30 | ||||
chr1:21345463-21345674 | Common:2; Rare:80 | ||||
chr1:23369807-23369866 | Rare:12 | ||||
chr1:23559422-23559643 | Common:1; Rare:94 | ||||
chr1:23778275-23778596 | Common:10; Rare:133 | ||||
chr1:23800752-23800948 | Common:1; Rare:66 | ||||
chr1:23959641-23959908 | Common:2; Rare:72 | ||||
chr1:23980241-23980468 | Rare:72 | ||||
chr1:24642890-24643329 | Common:2; Rare:146 | ||||
chr1:25232442-25232657 | Rare:87 |