Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:75710654-75711042 | Common:3; Rare:158 | ||||
chr2:84459219-84459585 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:85327916-85328050 | Common:1; Rare:62 | ||||
chr2:85354492-85354795 | Common:1; Rare:101 | ||||
chr2:85539068-85539172 | Common:1; Rare:40 | ||||
chr2:85561431-85561581 | Rare:56; Clinvar:4 | ||||
chr2:85595558-85595847 | Common:1; Rare:101 | ||||
chr2:85602350-85602483 | Common:1; Rare:26 | ||||
chr2:85602607-85602904 | Rare:79 | ||||
chr2:85603138-85603260 | Rare:28 | ||||
chr2:85611880-85612113 | Rare:104 | ||||
chr2:85753454-85753921 | Common:3; Rare:120 | ||||
chr2:85754041-85754152 | Rare:29 | ||||
chr2:86105843-86106266 | Common:3; Rare:123 | ||||
chr2:86195387-86195674 | Common:6; Rare:91 |