chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64791657147916572CG21GENIChomozygous114790707
64791669447916695GA25GENIChomozygous114790709
64791695747916958CT24GENIChomozygous114790711
64791714947917150CT18GENIChomozygous114790713
64791732047917321GA21GENIChomozygous114790715
64791735347917354GA28GENIChomozygous114790717
64791752447917525AG22GENIChomozygous114790719
64791766647917667GT7GENIChomozygous114790721
64791807647918077GA33GENIChomozygous114790725
64791850647918507GC20GENIChomozygous114790727
64791860847918609AC28GENIChomozygous114790729
64791886247918863GT23GENIChomozygous114790731
64791917747919178TC33GENIChomozygous114790733
64791945947919460GT28GENIChomozygous114790735
64791950347919504AG28GENIChomozygous114790737
64791998747919988TC26GENIChomozygous114790739
64792074047920741GA26GENIChomozygous114790741
64792110847921109GC27GENIChomozygous114790743
64792192347921924CT23GENIChomozygous114790745
64792218247922183AG37GENICheterozygous114790759
64792218947922190TC35GENICheterozygous114790761
64792221347922214GA34GENICpossibly homozygous114790767
64792223447922235CT33GENICheterozygous114790769
64792231347922314CT18GENIChomozygous114790771
64792243047922431GA22GENIChomozygous114790773
64792252547922526AT17GENIChomozygous114790775
64792264147922642CG29GENIChomozygous114790777
64792281847922819TA17GENIChomozygous114790779
64792283847922839TA15GENIChomozygous114790781
64792296047922961TC26GENIChomozygous114790783
64792314947923150CA22GENIChomozygous114790785
64792316047923161GA23GENIChomozygous114790787
64792320247923203AC24GENIChomozygous114790789
64792452747924528GA45GENIChomozygous114790791
64792471847924719GT34GENIChomozygous114790793
64792507047925071CT29GENIChomozygous114790795