chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64791657147916572CG31GENIChomozygous114790707
64791669447916695GA21GENIChomozygous114790709
64791695747916958CT46GENIChomozygous114790711
64791714947917150CT23GENIChomozygous114790713
64791752447917525AG23GENIChomozygous114790719
64791766647917667GT6GENIChomozygous114790721
64791807647918077GA57GENIChomozygous114790725
64791850647918507GC37GENIChomozygous114790727
64791860847918609AC39GENIChomozygous114790729
64791886247918863GT43GENIChomozygous114790731
64791917747919178TC41GENIChomozygous114790733
64791945947919460GT17GENIChomozygous114790735
64791950347919504AG24GENIChomozygous114790737
64791998747919988TC21GENICpossibly homozygous114790739
64792074047920741GA31GENIChomozygous114790741
64792110847921109GC45GENIChomozygous114790743
64792243047922431GA27GENIChomozygous114790773
64792252547922526AT36GENIChomozygous114790775
64792281847922819TA20GENIChomozygous114790779
64792283847922839TA18GENIChomozygous114790781
64792296047922961TC42GENIChomozygous114790783
64792314947923150CA36GENIChomozygous114790785
64792316047923161GA37GENIChomozygous114790787
64792320247923203AC39GENIChomozygous114790789
64792452747924528GA41GENIChomozygous114790791
64792471847924719GT52GENIChomozygous114790793
64792507047925071CT43GENIChomozygous114790795