Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:227563396-227563643 | Common:2; Rare:72 | ||||
chr1:227563716-227563988 | Common:2; Rare:83 | ||||
chr1:227728367-227728708 | Common:4; Rare:55 | ||||
chr1:227735179-227735574 | Common:5; Rare:204 | ||||
chr1:228082389-228082777 | Common:5; Rare:140 | ||||
chr1:228083481-228083699 | Rare:59 | ||||
chr1:228102356-228102551 | Rare:64 | ||||
chr1:228102897-228102968 | Common:1; Rare:19 | ||||
chr1:228103088-228103226 | Rare:53 | ||||
chr1:228103243-228103557 | Common:1; Rare:113 | ||||
chr1:228109188-228109515 | Rare:100 | ||||
chr1:228139813-228140438 | Common:4; Rare:185 | ||||
chr1:228140518-228140645 | Common:1; Rare:29 | ||||
chr1:228165390-228165639 | Rare:79 | ||||
chr1:228165710-228166077 | Common:1; Rare:144; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 |