Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74507669-74507820 | Rare:32 | ||||
chr2:74529642-74529997 | Rare:113; Clinvar:4; Clinvar (benign):1 | ||||
chr2:74958560-74958671 | Common:1; Rare:38 | ||||
chr2:75560888-75561014 | Rare:24 | ||||
chr2:85327919-85328137 | Common:3; Rare:99 | ||||
chr2:85354526-85354790 | Common:1; Rare:85 | ||||
chr2:85595546-85595764 | Common:2; Rare:66 | ||||
chr2:85602663-85602892 | Rare:57 | ||||
chr2:85612030-85612147 | Rare:28 | ||||
chr2:85616203-85616302 | Common:1; Rare:37 | ||||
chr2:86105810-86106247 | Common:2; Rare:127 | ||||
chr2:86195383-86195557 | Common:5; Rare:63 | ||||
chr2:88055730-88055935 | Rare:74 | ||||
chr2:88691474-88691798 | Common:2; Rare:126; Clinvar:1 | ||||
chr2:95165651-95165819 | Rare:49 |