Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52633581-52633625 | Rare:14 | ||||
chr1:52697418-52697677 | Common:2; Rare:51 | ||||
chr1:52697986-52698250 | Common:1; Rare:71 | ||||
chr1:52698267-52698516 | Common:3; Rare:83; Clinvar (pathogenic):1 | ||||
chr1:52726355-52726549 | Common:9; Rare:87 | ||||
chr1:52726732-52726788 | Rare:10 | ||||
chr1:52842579-52842908 | Common:8; Rare:112 | ||||
chr1:52921669-52921839 | Common:1; Rare:47 | ||||
chr1:52927170-52927358 | Common:4; Rare:58 | ||||
chr1:52927661-52927932 | Common:4; Rare:51 | ||||
chr1:53014876-53015059 | Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr1:53196627-53196929 | Common:1; Rare:108; Clinvar:6; Clinvar (benign):1 | ||||
chr1:53220212-53220444 | Rare:115 | ||||
chr1:53220512-53220780 | Common:3; Rare:118 | ||||
chr1:53238424-53238803 | Common:2; Rare:118 |