Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:225581286-225581418 | Common:1; Rare:22 | ||||
chr1:226943135-226943406 | Rare:48 | ||||
chr1:228368004-228368368 | Common:2; Rare:96 | ||||
chr1:228369116-228369482 | Common:1; Rare:79 | ||||
chr1:228370091-228370434 | Common:1; Rare:106 | ||||
chr1:228464612-228464814 | Rare:55 | ||||
chr1:229431960-229432747 | Common:5; Rare:204; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
chr1:229432750-229433130 | Common:4; Rare:91; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr1:229563730-229563925 | Common:2; Rare:21 | ||||
chr1:231422219-231422485 | Common:5; Rare:124; Clinvar:5; Clinvar (benign):5 | ||||
chr1:231812323-231812651 | Common:2; Rare:36 | ||||
chr1:231845367-231845587 | Common:2; Rare:41 | ||||
chr1:231847587-231847830 | Common:2; Rare:43 | ||||
chr1:232595415-232595571 | Common:5; Rare:38 | ||||
chr1:232630473-232630577 | Rare:33 |