Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74147840-74148058 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74178834-74179057 | Common:2; Rare:65 | ||||
chr2:74421639-74421768 | Rare:42 | ||||
chr2:74482921-74483115 | Common:1; Rare:69 | ||||
chr2:74507669-74507790 | Rare:25 | ||||
chr2:74529662-74530009 | Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74835149-74835294 | Rare:37 | ||||
chr2:74958872-74959071 | Rare:72 | ||||
chr2:84459231-84459572 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):4 | ||||
chr2:85327945-85328077 | Common:2; Rare:62 | ||||
chr2:85354517-85354790 | Common:1; Rare:90 | ||||
chr2:85602651-85602882 | Rare:58 | ||||
chr2:85612030-85612129 | Rare:25 | ||||
chr2:86105855-86106257 | Common:3; Rare:109 | ||||
chr2:86195395-86195674 | Common:6; Rare:91 |