Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19596580-19597295 | Common:5; Rare:211 | ||||
chr1:19597414-19597563 | Common:2; Rare:39 | ||||
chr1:19644170-19644338 | Common:2; Rare:45 | ||||
chr1:19799442-19799633 | Common:2; Rare:33 | ||||
chr1:19799635-19799780 | Common:1; Rare:39 | ||||
chr1:19799817-19800300 | Common:8; Rare:129 | ||||
chr1:19800435-19800550 | Rare:22 | ||||
chr1:19882211-19882543 | Common:3; Rare:98 | ||||
chr1:19882613-19882831 | Rare:49 | ||||
chr1:20508033-20508300 | Common:5; Rare:84 | ||||
chr1:20633893-20634094 | Rare:72 | ||||
chr1:20660883-20661085 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr1:20661289-20661803 | Common:3; Rare:178; Clinvar:4; Clinvar (benign):7 | ||||
chr1:20786243-20786322 | Common:1; Rare:20 | ||||
chr1:20786511-20786967 | Rare:166 |