chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145195721145195722AG52GENIChomozygous112870704
4145197271145197272AG51GENIChomozygous119315322
4145197305145197306TC46GENIChomozygous119315323
4145197918145197919AG61GENIChomozygous112870705
4145198516145198517TC47GENIChomozygous119315324
4145201312145201313TC28GENIChomozygous112870706
4145201765145201766TC51GENIChomozygous112870707
4145203093145203094CT44GENIChomozygous119315325
4145204160145204161CT54GENIChomozygous119315326
4145204570145204571AG54GENIChomozygous119412347
4145205104145205105AC54GENIChomozygous119315327
4145206300145206301AG62GENIChomozygous119315328
4145207559145207560CT52GENIChomozygous119315329
4145208138145208139TC56GENIChomozygous112870709
4145213384145213385TC42GENIChomozygous112870711
4145215748145215749TC35GENIChomozygous112870712
4145218784145218785AG50GENIChomozygous112870713
4145222351145222352TG68GENIChomozygous119315330
4145222743145222744TC58GENIChomozygous119315331
4145222926145222927TC50GENIChomozygous119315332
4145224901145224902CG26GENIChomozygous119315333
4145225194145225195TC56GENIChomozygous112870716
4145225273145225274CT47GENIChomozygous119315334
4145225920145225921AG62GENIChomozygous112870717
4145232701145232702GC66GENIChomozygous112870718
4145233671145233672CT59GENIChomozygous119315335
4145233918145233919TC65GENIChomozygous119315336
4145234556145234557CT67GENIChomozygous119315337
4145235080145235081TG61GENIChomozygous119315338
4145236330145236331TC54GENIChomozygous119315339
4145236399145236400AG60GENIChomozygous112870723
4145200837145200837T32GENICpossibly homozygous132967594
4145201749145201750A48GENICpossibly homozygous132967595
4145204337145204338T43GENIChomozygous132967596
4145215015145215015T47GENIChomozygous132967597
4145218831145218831AGT48GENIChomozygous132967598
4145236433145236434C52GENIChomozygous132967599
4145215025145215026AG45GENIChomozygous132973181