chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14782937247829373GA14GENIChomozygous146343848
14782943947829440GA14GENIChomozygous141206793
14782955547829556TC15GENIChomozygous141206794
14782972047829721AG20GENIChomozygous141206795
14782984847829849AG15GENIChomozygous141206796
14782987447829875TC17GENIChomozygous141206797
14783012247830123GA12GENIChomozygous141206798
14783034247830343GA15GENIChomozygous147904091
14783104547831046CT21GENIChomozygous141206800
14783107947831080AG21GENIChomozygous141206801
14783253047832531TC16GENIChomozygous146343852
14783311347833114TC21GENIChomozygous141206804
14783339547833396GT18GENIChomozygous141206805
14783350047833501AG25GENIChomozygous141206806
14783353647833537GC26GENIChomozygous141206807
14783383347833834AT21GENIChomozygous141206808
14783394447833945GA23GENIChomozygous141206809
14783162447831624AG15GENIChomozygous141160768
14783413947834140AT17GENIChomozygous141206810
14783421447834215CT19GENIChomozygous141206811
14783426747834272CTTCA20GENIChomozygous141160772
14783502847835029TC32GENIChomozygous141206812
14783525547835256T30GENIChomozygous141160773
14783526047835261GA30GENIChomozygous146343853
14783581047835811TC17GENIChomozygous146343854
14783616447836165AG18GENIChomozygous141206813
14783651447836515CT22GENIChomozygous141206814
14783657247836573CG21GENICpossibly homozygous141206815
14783599047835991AC20GENIChomozygous145259197