Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228082415-228082815 | Common:23; Rare:779 | ||||
chr1:228082846-228084332 | Common:18; Rare:807 | ||||
chr1:228102364-228103133 | Common:5; Rare:366 | ||||
chr1:228103091-228103210 | Rare:47 | ||||
chr1:228103121-228103770 | Common:7; Rare:774 | ||||
chr1:228108205-228108605 | Common:2; Rare:153 | ||||
chr1:228109169-228109576 | Rare:586 | ||||
chr1:228139760-228140403 | Common:20; Rare:924 | ||||
chr1:228140851-228141940 | Common:4; Rare:425 | ||||
chr1:228144723-228145458 | Common:3; Rare:206 | ||||
chr1:228145588-228146008 | Common:2; Rare:149 | ||||
chr1:228146862-228147944 | Common:4; Rare:362 | ||||
chr1:228165340-228166324 | Common:7; Rare:1292; Clinvar:23; Clinvar (benign):41; Clinvar (pathogenic):24 | ||||
chr1:228212967-228213247 | Rare:62 | ||||
chr1:228213565-228213965 | Common:16; Rare:416 |