Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:69452694-69452961 | Common:5; Rare:119 | ||||
chr15:70853325-70853420 | Rare:14 | ||||
chr15:72118151-72118458 | Common:2; Rare:97 | ||||
chr15:72231095-72231406 | Common:2; Rare:97 | ||||
chr15:72686172-72686238 | Common:2; Rare:29; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr15:72783475-72783660 | Rare:59 | ||||
chr15:73926268-73926704 | Rare:104 | ||||
chr15:73994584-73994801 | Common:1; Rare:46 | ||||
chr15:74173786-74173821 | Common:1; Rare:11 | ||||
chr15:74461077-74461314 | Common:1; Rare:73 | ||||
chr15:74615727-74615891 | Common:2; Rare:51 | ||||
chr15:74938018-74938265 | Common:2; Rare:88 | ||||
chr15:75455764-75455957 | Rare:62 | ||||
chr15:75647870-75647948 | Common:1; Rare:13 | ||||
chr15:76336479-76336828 | Common:2; Rare:85 |