chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173025815173025816AG33GENIChomozygous114093997
5173026554173026555GA29GENIChomozygous114293081
5173028708173028709CT29GENIChomozygous114293083
5173030136173030137AC45GENICpossibly homozygous114293085
5173031125173031126AG40GENIChomozygous114094003
5173031888173031889AG35GENIChomozygous114094005
5173033324173033325GT23GENIChomozygous114094007
5173033345173033346CT34GENIChomozygous114094008
5173039133173039134AG25GENIChomozygous114094016
5173040172173040173AG22GENIChomozygous114094018
5173040725173040726GA25GENIChomozygous114293087
5173041720173041721GA22GENIChomozygous114094020
5173043430173043431TA18GENIChomozygous114456429
5173043431173043432AT18GENIChomozygous118848144
5173046112173046113TC23GENIChomozygous114094022
5173047119173047120GA45GENIChomozygous114094024
5173048699173048700GA41GENIChomozygous114293091
5173048772173048773CG17GENIChomozygous114293093
5173049728173049729AG47GENIChomozygous114094026