Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25232407-25232727 | Rare:116 | ||||
chr1:25246694-25246751 | Rare:24 | ||||
chr1:25246899-25247218 | Common:1; Rare:112 | ||||
chr1:25247294-25247900 | Common:6; Rare:202 | ||||
chr1:25337803-25337983 | Rare:24 | ||||
chr1:25338286-25338653 | Common:4; Rare:108 | ||||
chr1:25338770-25338946 | Common:1; Rare:37 | ||||
chr1:25430070-25430580 | Common:6; Rare:141 | ||||
chr1:25430822-25431177 | Common:3; Rare:129 | ||||
chr1:25431239-25431506 | Common:1; Rare:71 | ||||
chr1:25543454-25543699 | Common:1; Rare:93; Clinvar:5 | ||||
chr1:25543755-25543834 | Rare:24; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr1:25543840-25543937 | Common:1; Rare:21 | ||||
chr1:25800008-25800429 | Common:1; Rare:142; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
chr1:25800447-25800471 | Rare:5 |