Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20661406-20661709 | Common:1; Rare:109; Clinvar:3; Clinvar (benign):4 | ||||
chr1:21345502-21345655 | Rare:57 | ||||
chr1:23559391-23559671 | Common:2; Rare:123 | ||||
chr1:23959641-23959849 | Common:2; Rare:54 | ||||
chr1:23980279-23980603 | Common:1; Rare:101 | ||||
chr1:24642909-24643242 | Rare:103 | ||||
chr1:25232464-25232582 | Rare:43 | ||||
chr1:25338214-25338424 | Common:1; Rare:75 | ||||
chr1:25819885-25820009 | Common:2; Rare:33 | ||||
chr1:25859353-25859578 | Common:3; Rare:94 | ||||
chr1:26279941-26280158 | Rare:126 | ||||
chr1:26432123-26432350 | Common:4; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26900428-26900543 | Rare:40 | ||||
chr1:28505861-28506050 | Common:1; Rare:78 | ||||
chr1:28552829-28553113 | Common:2; Rare:105 |