chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157573007157573008GT50GENIChomozygous137248641
4157573411157573412TC26GENIChomozygous137248642
4157573815157573816AG45GENIChomozygous137248643
4157574484157574485AG65GENIChomozygous137248644
4157574676157574677G70GENIChomozygous136925232
4157575495157575496GA48GENIChomozygous137248645
4157575899157575900TG31GENIChomozygous137248646
4157576154157576155GA33GENIChomozygous137248647
4157577553157577554AG49GENIChomozygous137248648
4157577766157577767TC45GENIChomozygous137248649
4157578718157578722TTGT21GENICpossibly homozygous136925233
4157580326157580327AG36GENIChomozygous137248650