chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4104423873104423874AG55GENIChomozygous137186374
4104423928104423929GC57GENICpossibly homozygous137186375
4104426042104426043TC66GENIChomozygous137186376
4104426636104426637GA68GENIChomozygous137186377
4104428550104428550C24GENIChomozygous136909095
4104428805104428806TC46GENIChomozygous137186378
4104429285104429286TA23GENIChomozygous137186379
4104429289104429290TA23GENIChomozygous137186380
4104429977104429978GA52GENIChomozygous137186381
4104430572104430573GA56GENIChomozygous137186382
4104430776104430777C53GENIChomozygous136909096
4104430998104430999GC38GENIChomozygous137186383
4104431071104431072T39GENIChomozygous136909097
4104431804104431805GT76GENIChomozygous137186384
4104432110104432111GA71GENIChomozygous137186385
4104432317104432318AT58GENIChomozygous137186386
4104432900104432900TC57GENICpossibly homozygous136909098
4104434705104434706AG65GENIChomozygous137186387
4104434743104434744TC63GENIChomozygous137186388
4104434746104434746A63GENIChomozygous136909099