Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:220046401-220046841 | Common:1; Rare:126 | ||||
chr1:220089729-220090002 | Common:1; Rare:64 | ||||
chr1:220093979-220094250 | Common:2; Rare:94; Clinvar (benign):2 | ||||
chr1:220094269-220094318 | Rare:18; Clinvar (pathogenic):1 | ||||
chr1:220094421-220094445 | Rare:7; Clinvar (benign):1 | ||||
chr1:220094450-220094591 | Rare:44; Clinvar (benign):2 | ||||
chr1:220271886-220272226 | Common:3; Rare:89 | ||||
chr1:220272327-220272682 | Rare:102; Clinvar:5 | ||||
chr1:220272829-220272841 | |||||
chr1:220690176-220690473 | Rare:110 | ||||
chr1:220748083-220748397 | Common:3; Rare:69 | ||||
chr1:220786693-220787032 | Common:5; Rare:86 | ||||
chr1:220787126-220787189 | Rare:20 | ||||
chr1:221742033-221742467 | Common:4; Rare:108 | ||||
chr1:222589608-222589638 | Common:1; Rare:6 |