Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42817236-42817460 | Rare:86 | ||||
chr1:42846399-42846638 | Common:1; Rare:67 | ||||
chr1:42958800-42959066 | Common:3; Rare:74; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43367953-43368235 | Rare:75 | ||||
chr1:43389757-43389964 | Common:4; Rare:92 | ||||
chr1:43946574-43946983 | Rare:108 | ||||
chr1:44031410-44031488 | Common:1; Rare:17 | ||||
chr1:44218405-44218702 | Rare:101 | ||||
chr1:44674451-44674739 | Common:2; Rare:64 | ||||
chr1:44775469-44775599 | Rare:53 | ||||
chr1:44775835-44776138 | Common:2; Rare:110 | ||||
chr1:45012179-45012268 | Rare:35; Clinvar:4 | ||||
chr1:45339996-45340178 | Rare:54 | ||||
chr1:45340369-45340480 | Common:2; Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
chr1:45500005-45500335 | Common:2; Rare:75; Clinvar:4; Clinvar (pathogenic):2 |