Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:69160336-69160662 | Common:4; Rare:101 | ||||
chr15:69298793-69298940 | Common:3; Rare:33 | ||||
chr15:69414209-69414465 | Rare:88 | ||||
chr15:69452774-69453020 | Common:5; Rare:109 | ||||
chr15:69453496-69453716 | Common:2; Rare:64 | ||||
chr15:70763367-70763693 | Common:2; Rare:104 | ||||
chr15:70853949-70854284 | Rare:98 | ||||
chr15:70892381-70892851 | Common:1; Rare:105 | ||||
chr15:72117966-72118425 | Common:5; Rare:157 | ||||
chr15:72231107-72231523 | Common:3; Rare:134 | ||||
chr15:72375944-72376137 | Common:2; Rare:80; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
chr15:72474210-72474555 | Rare:115 | ||||
chr15:72686173-72686225 | Common:2; Rare:23; Clinvar:2; Clinvar (benign):2 | ||||
chr15:73926313-73926482 | Rare:47 | ||||
chr15:73994595-73994806 | Rare:45 |