Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145996555-145996848 | Common:1; Rare:113 | ||||
chr1:146938315-146938343 | Rare:14 | ||||
chr1:147172420-147172744 | Common:1; Rare:86 | ||||
chr1:147541307-147541592 | Common:1; Rare:50 | ||||
chr1:148458639-148459006 | Common:2; Rare:91 | ||||
chr1:148952233-148952642 | Common:5; Rare:107 | ||||
chr1:149812225-149812527 | Common:2; Rare:141 | ||||
chr1:149842748-149842921 | Rare:3 | ||||
chr1:149850845-149851062 | Rare:1 | ||||
chr1:149886663-149886959 | Rare:100 | ||||
chr1:149887900-149888191 | Rare:92 | ||||
chr1:149917795-149917916 | Rare:35 | ||||
chr1:149927775-149927855 | Rare:28; Clinvar (benign):3 | ||||
chr1:150010697-150010837 | Common:1; Rare:34 | ||||
chr1:150067649-150067860 | Rare:64 |