Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119140634-119140730 | Rare:27 | ||||
chr1:145823895-145824219 | Rare:114 | ||||
chr1:145918680-145919002 | Common:2; Rare:70 | ||||
chr1:145927359-145927591 | Common:1; Rare:57; Clinvar (pathogenic):1 | ||||
chr1:145964575-145964737 | Rare:41 | ||||
chr1:145995992-145996134 | Rare:60 | ||||
chr1:145996144-145996615 | Common:1; Rare:183 | ||||
chr1:147172429-147172779 | Common:1; Rare:90 | ||||
chr1:149812358-149812611 | Common:1; Rare:70 | ||||
chr1:149886208-149886255 | Rare:21 | ||||
chr1:149886646-149886924 | Common:1; Rare:90 | ||||
chr1:149887914-149888222 | Rare:91 | ||||
chr1:149927760-149927900 | Common:1; Rare:58; Clinvar (benign):4 | ||||
chr1:149931395-149931650 | Common:1; Rare:60 | ||||
chr1:150067682-150067858 | Rare:56 |