Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119648097-119648350 | Common:3; Rare:89 | ||||
chr1:120176273-120176565 | Rare:61 | ||||
chr1:145773348-145773860 | Common:4; Rare:87 | ||||
chr1:145823788-145824297 | Rare:182 | ||||
chr1:145836588-145836867 | Common:1; Rare:72 | ||||
chr1:145845352-145845636 | Common:4; Rare:65 | ||||
chr1:145918657-145919020 | Common:2; Rare:91; Clinvar:1 | ||||
chr1:145925795-145926138 | Common:2; Rare:102; Clinvar:1 | ||||
chr1:145927135-145927308 | Common:1; Rare:32; Clinvar (benign):1 | ||||
chr1:145927354-145927612 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145957996-145958202 | Rare:47 | ||||
chr1:145964567-145964747 | Rare:46 | ||||
chr1:145996453-145996735 | Common:1; Rare:106 | ||||
chr1:147172009-147172290 | Rare:81 | ||||
chr1:147172322-147172354 | Rare:8 |