Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20185983-20186183 | Common:2; Rare:67 | ||||
chr1:20186446-20186555 | Common:1; Rare:15 | ||||
chr1:20290797-20290936 | Common:3; Rare:36 | ||||
chr1:20302963-20303126 | Common:3; Rare:35 | ||||
chr1:20508045-20508216 | Common:2; Rare:61 | ||||
chr1:20661211-20661245 | Rare:11 | ||||
chr1:20661283-20661724 | Common:4; Rare:158; Clinvar:4; Clinvar (benign):8 | ||||
chr1:20732053-20732297 | Common:1; Rare:52 | ||||
chr1:20786557-20786690 | Rare:35 | ||||
chr1:20786695-20786832 | Rare:57 | ||||
chr1:20786834-20786859 | Rare:9 | ||||
chr1:20787196-20787399 | Rare:102 | ||||
chr1:21174734-21174821 | Rare:14 | ||||
chr1:21176848-21177113 | Rare:78 | ||||
chr1:21177283-21177434 | Rare:16 |