chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107087249270872500GTGTGTGT--------22GENICheterozygous52803539
107087497670874977AG39GENIChomozygous51489546
107087253470872535GA27GENICpossibly homozygous52764350
107087280470872805AG39GENIChomozygous51489542
107087387570873876AG24GENIChomozygous51489543
107087387870873879TC25GENIChomozygous51489544
107087487570874876GA38GENIChomozygous51489545
107087497970874980GA37GENIChomozygous51489547
107087519170875192GGTTT25GENICheterozygous51489548
107087519170875192GGTT25GENICheterozygous51489549
107087519170875192GGTTTT25GENICheterozygous52384148
107087540170875402AG29GENIChomozygous51489550
107087553470875536GT--13GENICpossibly homozygous52461238
107087577370875774TC29GENIChomozygous51489554
107087630770876308AG42GENIChomozygous51489555
107087637770876378CCAGG42GENIChomozygous51489556
107087658870876589TA33GENIChomozygous51489557
107087679170876792AAG25GENIChomozygous51489558
107087727970877280GA38GENIChomozygous51489559
107087796870877969TC39GENIChomozygous51489560
107087808370878084GT24GENIChomozygous51489561
107087888570878886GA36GENIChomozygous51489564
107087998670879987AG25GENIChomozygous51489565
107088013870880140AA--16GENIChomozygous51489566
107088016170880162AG25GENIChomozygous51489567
107088079370880794CT36GENIChomozygous51489568
107088271570882716AG36GENIChomozygous51489569
107088323970883240CT44GENIChomozygous51489570
107088356170883562CCTTTTTT7GENICheterozygous52384152
107088358070883590GCTTATTTGG----------11GENICheterozygous52384153
107088376870883780TTTTTTTTTTTT------------8GENICpossibly homozygous51489572
107088584370885850TTGTGTC-------43GENIChomozygous51489574