chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2236512100236512101GA27GENIChomozygous111029173
2236512676236512677TC52GENICpossibly homozygous111029175
2236512712236512713CT50GENIChomozygous111029177
2236513172236513173TC41GENIChomozygous120327099
2236513186236513187CT39GENIChomozygous120327100
2236513214236513215AG44GENIChomozygous111029185
2236513378236513379CA45GENICpossibly homozygous120327101
2236513413236513414GA45GENIChomozygous120327102
2236513816236513817TC35GENIChomozygous120327103
2236513820236513821TC35GENIChomozygous120327104
2236513825236513826AC38GENIChomozygous120327105
2236514237236514238AG27GENIChomozygous110319717
2236514291236514292GC13GENIChomozygous110319719