Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:73737266-73737589 | Common:3; Rare:107 | ||||
chr2:73828798-73829037 | Common:1; Rare:54 | ||||
chr2:73892744-73893051 | Common:2; Rare:54 | ||||
chr2:73926735-73926936 | Common:2; Rare:105; Clinvar:7; Clinvar (benign):3 | ||||
chr2:74147849-74148145 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74178784-74179047 | Common:3; Rare:74 | ||||
chr2:74198440-74198637 | Rare:78 | ||||
chr2:74290266-74290469 | Rare:35 | ||||
chr2:74290519-74290731 | Common:2; Rare:35 | ||||
chr2:74421579-74421759 | Rare:62 | ||||
chr2:74440419-74440759 | Rare:86 | ||||
chr2:74458095-74458666 | Common:2; Rare:184 | ||||
chr2:74465350-74465439 | Rare:24; Clinvar:1 | ||||
chr2:74472353-74472758 | Common:4; Rare:186 | ||||
chr2:74482728-74483129 | Common:1; Rare:140 |