Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:65792288-65792447 | Common:1; Rare:38 | ||||
chr15:66386686-66386936 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):3 | ||||
chr15:66504786-66505161 | Common:2; Rare:140 | ||||
chr15:67254627-67254813 | Rare:67 | ||||
chr15:69414109-69414366 | Rare:71 | ||||
chr15:70763406-70763840 | Common:2; Rare:140 | ||||
chr15:70854034-70854281 | Rare:74 | ||||
chr15:70892403-70892616 | Common:1; Rare:50 | ||||
chr15:72118190-72118425 | Common:2; Rare:71 | ||||
chr15:72231114-72231520 | Common:3; Rare:129 | ||||
chr15:72375944-72376118 | Common:2; Rare:77; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
chr15:73633215-73633420 | Rare:90 | ||||
chr15:73926322-73926482 | Rare:45 | ||||
chr15:73994606-73994806 | Rare:44 | ||||
chr15:74461107-74461307 | Rare:62 |