chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157573007157573008GT11GENIChomozygous137248641
4157573411157573412TC17GENIChomozygous137248642
4157573815157573816AG14GENIChomozygous137248643
4157574484157574485AG14GENIChomozygous137248644
4157575495157575496GA24GENIChomozygous137248645
4157575899157575900TG11GENIChomozygous137248646
4157576154157576155GA20GENIChomozygous137248647
4157577553157577554AG26GENIChomozygous137248648
4157577766157577767TC18GENIChomozygous137248649
4157580326157580327AG22GENIChomozygous137248650
4157574676157574677G21GENIChomozygous136925232
4157578718157578722TTGT6GENIChomozygous136925233