chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71225900712259008CG38GENIChomozygous116274512
71225905212259053TC36GENIChomozygous116274514
71226051012260511GT30GENICheterozygous116274516
71226067512260676GA35GENIChomozygous116274518
71226142612261427AG26GENIChomozygous115569720
71226295812262959GA41GENIChomozygous116274520
71226331212263313AG37GENIChomozygous116274522
71226486112264862AG30GENIChomozygous116274524
71226500112265002TC32GENIChomozygous116274526
71226501812265019AG31GENIChomozygous115569725
71226674112266742GA35GENIChomozygous116274528
71226708012267081AG44GENICpossibly homozygous116274530
71226835612268357AT31GENIChomozygous116274532
71227113412271135AG31GENIChomozygous116274534
71227127512271276TC30GENIChomozygous115569728
71227322912273230TC29GENIChomozygous115569729
71227381012273811CG30GENIChomozygous115569730
71227455112274552TG28GENIChomozygous115569731
71227487212274873AG31GENIChomozygous115569732
71227535012275351CT24GENIChomozygous115569733
71227543212275433TC28GENIChomozygous115569734
71227561112275612TC30GENIChomozygous115569735
71227569712275698TC39GENIChomozygous115569736
71227570012275701TG42GENIChomozygous115569737
71227571012275711CG45GENIChomozygous115569738
71227633412276335TC37GENICpossibly homozygous115569739
71227774512277746GT45GENIChomozygous115569740
71227860512278606CT36GENIChomozygous115569741
71227878012278781TC25GENIChomozygous115569742
71227925212279253AG36GENIChomozygous115569744
71228014812280149CA37GENIChomozygous115569745
71228027612280277CT32GENIChomozygous115569746