chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28674203286742033AG55GENIChomozygous136203741
28674252986742530GA62GENIChomozygous144303200
28674283486742835TG59GENIChomozygous136203742
28674334086743341CG23GENICheterozygous144303202
28674334286743343CG24GENICpossibly homozygous144303203
28674334486743345CG24GENICpossibly homozygous144303204
28674499086744991GA32GENIChomozygous144303205
28674654686746547TC57GENIChomozygous136203743
28674656486746565GT56GENIChomozygous136203744
28674667586746676GA47GENIChomozygous136203745
28674830986748310TC36GENIChomozygous136203748
28674947786749478TC53GENIChomozygous136203750
28675017986750180GA54GENIChomozygous136203751
28675025786750258TA49GENIChomozygous136203752
28675067386750674AG62GENIChomozygous136203755
28675067786750678TC63GENIChomozygous136203756
28675108786751088TG48GENIChomozygous136203758
28675114686751147AG54GENIChomozygous136203759
28675148086751481AG68GENIChomozygous136203760
28675226686752267AC61GENIChomozygous136203762
28675260086752601GT41GENIChomozygous144303206
28675269786752698GA50GENIChomozygous144303207
28675307886753079TC34GENIChomozygous136203763
28675312286753123CA40GENIChomozygous144303208
28674322986743229TC31GENICpossibly homozygous144273246
28674662086746620T52GENIChomozygous135924862
28674972386749723T56GENIChomozygous135924864
28675225586752257AA55GENIChomozygous144273247
28675417186754195ATGGCCAGCTTCTTTGTCACCCTC53GENIChomozygous135924865
28675420786754208A55GENIChomozygous135924866
28675439786754398T57GENIChomozygous135924867
28675448386754484TC66GENIChomozygous136203764
28675480186754802GA59GENIChomozygous144303209
28675491586754916T57GENICpossibly homozygous135924868
28675620886756209GT63GENICpossibly homozygous136203766