chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4104423873104423874AG60GENIChomozygous137186374
4104423928104423929GC62GENIChomozygous137186375
4104424268104424269GA43GENIChomozygous148877375
4104426042104426043TC66GENIChomozygous137186376
4104426636104426637GA52GENIChomozygous137186377
4104428805104428806TC36GENIChomozygous137186378
4104429285104429286TA23GENIChomozygous137186379
4104429289104429290TA24GENIChomozygous137186380
4104429977104429978GA43GENIChomozygous137186381
4104430572104430573GA43GENIChomozygous137186382
4104430998104430999GC32GENIChomozygous137186383
4104431804104431805GT47GENIChomozygous137186384
4104432110104432111GA55GENIChomozygous137186385
4104432317104432318AT50GENIChomozygous137186386
4104434705104434706AG54GENIChomozygous137186387
4104434743104434744TC54GENICpossibly homozygous137186388
4104428550104428550C2GENICheterozygous136909095
4104430776104430777C44GENIChomozygous136909096
4104431071104431072T31GENIChomozygous136909097
4104432900104432900TC36GENICheterozygous136909098
4104434746104434746A53GENICpossibly homozygous136909099