chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1145760983145760984GA29GENIChomozygous60883866
1145761102145761103TA19GENIChomozygous60883867
1145761116145761117CT17GENIChomozygous60883868
1145761596145761597GGTCTC37GENICpossibly homozygous60883869
1145761596145761597GGTC37GENICheterozygous61304860
1145763199145763200AG36GENIChomozygous60883870
1145763222145763223TC25GENIChomozygous60883871