Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74147875-74148042 | Common:1; Rare:42; Clinvar:2 | ||||
chr2:74421609-74421771 | Rare:52 | ||||
chr2:74482982-74483095 | Rare:40 | ||||
chr2:74529659-74529964 | Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
chr2:75560916-75561045 | Rare:29 | ||||
chr2:75561295-75561430 | Common:1; Rare:17 | ||||
chr2:84459237-84459581 | Common:3; Rare:85; Clinvar:4; Clinvar (benign):4 | ||||
chr2:85327951-85328066 | Common:1; Rare:54 | ||||
chr2:85354526-85354790 | Common:1; Rare:85 | ||||
chr2:85595430-85595772 | Common:3; Rare:106 | ||||
chr2:85612030-85612103 | Rare:19 | ||||
chr2:85616000-85616192 | Rare:69 | ||||
chr2:86105843-86106253 | Common:3; Rare:112 | ||||
chr2:86195392-86195532 | Common:4; Rare:51 | ||||
chr2:88691462-88691696 | Common:2; Rare:76 |