chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143595239143595240TA14GENIChomozygous56962816
4143595754143595755AG18GENIChomozygous56962817
4143596309143596310GA7GENICheterozygous56962819
4143597231143597232AAATAT1GENIChomozygous56962820
4143597443143597444AT23GENICpossibly homozygous56962821
4143598137143598138GGA2GENIChomozygous56962822
4143598221143598222CA20GENIChomozygous56962823
4143598596143598597CT8GENIChomozygous56962824
4143599907143599908TC26GENIChomozygous56962825
4143603066143603067A-4GENIChomozygous56962827
4143604389143604390TC11GENICheterozygous56962828
4143604440143604441C-9GENIChomozygous56962829
4143605245143605246AATT3GENIChomozygous56962830
4143605468143605469GT3GENICheterozygous56962831
4143606108143606109CCT7GENICpossibly homozygous56962832
4143606224143606225AG3GENIChomozygous56962833
4143606248143606249TC4GENIChomozygous56962834
4143606935143606936TG13GENICheterozygous56962835
4143606958143606961CCC---6GENICheterozygous56962837
4143607052143607053T-2GENICheterozygous56962838
4143609308143609309AAT1GENIChomozygous56962839
4143609647143609650ACG---1GENIChomozygous56962840
4143610355143610356AG18GENICpossibly homozygous56962841
4143610545143610546CA18GENIChomozygous56962842
4143610766143610767GA16GENIChomozygous56962843
4143611578143611579A-7GENICpossibly homozygous56962845
4143613236143613237AT6GENICheterozygous56962849