Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185156700-185156814 | Common:1; Rare:45 | ||||
chr1:185156916-185157303 | Common:1; Rare:109 | ||||
chr1:185157420-185157527 | Common:1; Rare:35 | ||||
chr1:185317206-185317468 | Common:1; Rare:79 | ||||
chr1:186375104-186375892 | Common:1; Rare:220 | ||||
chr1:186680294-186680691 | Common:3; Rare:91 | ||||
chr1:190474716-190474883 | Common:1; Rare:38 | ||||
chr1:190475790-190475913 | Common:2; Rare:32 | ||||
chr1:192808619-192808787 | Common:1; Rare:37 | ||||
chr1:192808794-192809175 | Common:4; Rare:159; Clinvar:1 | ||||
chr1:193059309-193059677 | Rare:174 | ||||
chr1:193121764-193122248 | Common:2; Rare:172; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr1:193186578-193186683 | Rare:15 | ||||
chr1:198156935-198157287 | Rare:116 | ||||
chr1:201739742-201739932 | Rare:38 |