chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1192300338192300339AG27GENIChomozygous61574536
1192300595192300596GA41GENIChomozygous61025806
1192300638192300639GGGTGT20GENIChomozygous61025808
1192300888192300890CG--23GENIChomozygous61025809
1192300938192300939TC25GENICpossibly homozygous61025811
1192301009192301010CT16GENIChomozygous61025812
1192301498192301499TC30GENIChomozygous61025813
1192301713192301714AACTC37GENIChomozygous61025814
1192301903192301904GA24GENIChomozygous61025815
1192301965192301966AAT24GENIChomozygous61025816