Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:100430957-100431068 | Rare:18 | ||||
chr8:102108081-102108291 | Common:2; Rare:45 | ||||
chr8:102808516-102808728 | Rare:37 | ||||
chr8:110210822-110211045 | Common:1; Rare:37 | ||||
chr8:123653700-123653977 | Rare:49 | ||||
chr8:127737531-127737794 | Common:2; Rare:69 | ||||
chr8:133256805-133257063 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
chr8:143281630-143281799 | Common:3; Rare:41 | ||||
chr8:145002816-145003035 | Common:2; Rare:79 | ||||
chr9:738043-738429 | Common:4; Rare:155; Clinvar:1 | ||||
chr9:15468961-15469283 | Common:2; Rare:102 | ||||
chr9:15469949-15470180 | Rare:71 | ||||
chr9:34380793-34380900 | Common:1; Rare:35 | ||||
chr9:35684247-35684561 | Rare:71; Clinvar:3; Clinvar (benign):4 | ||||
chr9:35720135-35720440 | Rare:79 |