Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36397822-36398015 | Common:3; Rare:47 | ||||
chr1:36450431-36450590 | Common:1; Rare:48 | ||||
chr1:36464236-36464492 | Common:2; Rare:75 | ||||
chr1:36467228-36467484 | Rare:50 | ||||
chr1:36472280-36472703 | Common:3; Rare:129; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:36473557-36473923 | Common:3; Rare:99; Clinvar (benign):1 | ||||
chr1:36478742-36479096 | Common:2; Rare:64 | ||||
chr1:36481920-36482208 | Rare:45 | ||||
chr1:36482735-36482965 | Common:2; Rare:48 | ||||
chr1:36482967-36483003 | Rare:12 | ||||
chr1:36483010-36483068 | Rare:10 | ||||
chr1:36483070-36483278 | Rare:29 | ||||
chr1:37474359-37474595 | Common:1; Rare:95 | ||||
chr1:37514727-37514828 | Rare:66 | ||||
chr1:37692204-37692569 | Common:4; Rare:84 |