chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
674793597479360CT29GENIChomozygous798688113
674807087480709GT38GENIChomozygous798688114
674814457481446AG31GENIChomozygous798688115
674816957481696CT24GENIChomozygous798688116
674817667481767GA32GENIChomozygous798688117
674831777483178TC36GENIChomozygous798688118
674834097483410TA35GENICpossibly homozygous798688119
674847187484719CG45GENICheterozygous798688120
674848147484815TC40GENIChomozygous798688121
674864717486472AT30GENIChomozygous798688122
674865167486517GC23GENIChomozygous798688123
674874357487436AG31GENICpossibly homozygous798688124
674891547489155AG30GENIChomozygous798688125
674891597489160TA28GENIChomozygous798688126
674893107489311AT30GENIChomozygous798688127
674893117489312GC30GENIChomozygous798688128
674907487490749AG44GENICpossibly homozygous798688129
674911477491148AG36GENIChomozygous798688130
674911497491150GA36GENIChomozygous798688131
674922767492277CT11GENIChomozygous798688132