Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23791674-23791975 | Rare:41 | ||||
chr1:23793018-23793171 | Common:1; Rare:48 | ||||
chr1:23799485-23799685 | Common:1; Rare:33 | ||||
chr1:23800705-23800957 | Common:1; Rare:86 | ||||
chr1:23825356-23825562 | Common:3; Rare:65; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr1:23959090-23959347 | Common:3; Rare:54 | ||||
chr1:23959640-23959946 | Common:2; Rare:77 | ||||
chr1:23977047-23977157 | Rare:22 | ||||
chr1:23979304-23979499 | Rare:34 | ||||
chr1:23980239-23980564 | Common:1; Rare:104 | ||||
chr1:24415633-24415882 | Common:1; Rare:63 | ||||
chr1:24642876-24643582 | Common:4; Rare:243 | ||||
chr1:24744994-24745623 | Common:5; Rare:215 | ||||
chr1:25232448-25232662 | Rare:85 | ||||
chr1:25247419-25247642 | Common:2; Rare:86 |