chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3147503976147503977AAT31GENICpossibly homozygous57727510
3147506046147506052GCTGCT------3GENICheterozygous58561950
3147506049147506052GCT---3GENICheterozygous58752767
3147506245147506246GA7GENIChomozygous57727514
3147506708147506709CCT34GENIChomozygous57727516
3147507467147507468CG33GENIChomozygous57727518
3147506436147506437CG32GENICheterozygous58224920
3147507762147507763T-13GENIChomozygous57727520
3147508105147508106GA22GENICpossibly homozygous57727522
3147508526147508527GT17GENIChomozygous57727524
3147514505147514506CG14GENICpossibly homozygous57727530
3147515147147515148TG30GENIChomozygous57727532
3147515346147515347TC45GENIChomozygous57727534
3147515848147515849AAT15GENICheterozygous59049948
3147515841147515842CCTTTTTTT17GENICheterozygous59049942
3147515844147515845AATTTTTTT17GENICheterozygous59049944
3147515845147515846AATT16GENICheterozygous59049946
3147515853147515854GT13GENICheterozygous59049950
3147515858147515859CT14GENICheterozygous59049952
3147516163147516164AG15GENICpossibly homozygous57727540
3147515950147515955TCTCT-----9GENICpossibly homozygous58810015