chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157573007157573008GT59GENIChomozygous137248641
4157573411157573412TC41GENIChomozygous137248642
4157573815157573816AG43GENIChomozygous137248643
4157574484157574485AG56GENIChomozygous137248644
4157574676157574677G54GENICpossibly homozygous136925232
4157575495157575496GA54GENIChomozygous137248645
4157575899157575900TG35GENIChomozygous137248646
4157576154157576155GA50GENIChomozygous137248647
4157577553157577554AG61GENIChomozygous137248648
4157577766157577767TC47GENIChomozygous137248649
4157578718157578722TTGT19GENIChomozygous136925233
4157580326157580327AG48GENIChomozygous137248650