chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135266403852664039TC16GENIChomozygous50361143
135266440352664404CT23GENIChomozygous50361145
135266739752667398AAT20GENICpossibly homozygous49948491
135267122052671221TC17GENIChomozygous49948524
135267162252671623TC24GENIChomozygous49948527
135267164352671644CA19GENIChomozygous49948528
135267165352671654CT19GENIChomozygous49948529
135267201852672019GT18GENIChomozygous49948531
135267220452672205TA9GENIChomozygous49948532
135267224652672247CT14GENIChomozygous49948533
135267230552672306TC18GENIChomozygous50361147
135267811252678113AAT11GENIChomozygous49758278
135267812252678123A-14GENIChomozygous49758279
135267812852678129CCA15GENIChomozygous49758280