chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142689059142689060CT28GENICpossibly homozygous114033890
5142689482142689483AG17GENIChomozygous114150824
5142689484142689485A17GENIChomozygous128248635
5142689616142689617AG17GENIChomozygous114033891
5142689912142689913CT26GENIChomozygous114033892
5142690107142690108GT20GENIChomozygous114033893
5142690136142690136T18GENIChomozygous128248636
5142690338142690339CT18GENIChomozygous114033894
5142690714142690715AG25GENIChomozygous114033895
5142690719142690720CT26GENIChomozygous114033896
5142690903142690904CT17GENIChomozygous114033897
5142691300142691301AC6GENIChomozygous114033898
5142691316142691316C5GENIChomozygous128248637
5142691640142691640GCTACTGCGA20GENIChomozygous128248638
5142692042142692043AC11GENIChomozygous114033899
5142692740142692741TC18GENIChomozygous114033901
5142692964142692965AG23GENIChomozygous114033902
5142693280142693281GA16GENIChomozygous114033903
5142693686142693687CT20GENIChomozygous114033904
5142694796142694797CT29GENIChomozygous114033905
5142695469142695470GA25GENIChomozygous114033906
5142695901142695902TC19GENIChomozygous114033907
5142696239142696240TC23GENIChomozygous114033908