chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107087247870872500GTGTGTGTGTGTGTGTGTGTGT----------------------5GENICheterozygous52725066
107087280470872805AG17GENIChomozygous51489542
107087387570873876AG28GENIChomozygous51489543
107087387870873879TC26GENIChomozygous51489544
107087519170875192GGTTT10GENICheterozygous51489548
107087519170875192GGTT10GENICheterozygous51489549
107087540170875402AG18GENIChomozygous51489550
107087557170875577TGTGTA------11GENICheterozygous52725068
107087596370875964GA24GENIChomozygous52160618
107087609870876099TTG9GENIChomozygous52160619
107087616670876167GA17GENIChomozygous51689620
107087630770876308AG22GENIChomozygous51489555
107087637770876378CCAGG19GENIChomozygous51489556
107087658870876589TA23GENIChomozygous51489557
107087679170876792AAG27GENIChomozygous51489558
107087727970877280GA10GENIChomozygous51489559
107087770770877708AT17GENIChomozygous51689624
107087812270878123AATTCTTTCTTTCT4GENIChomozygous52725070
107087824670878247CT19GENIChomozygous52160621
107087899270878993GT15GENIChomozygous52160622
107088013870880140AA--8GENICpossibly homozygous51489566
107088013970880140A-8GENICheterozygous52384150
107088016170880162AG14GENIChomozygous51489567
107088152770881528GA14GENIChomozygous52160623
107088175670881757AG23GENIChomozygous52160624
107088263970882640GA28GENIChomozygous52160625
107088297670882977GA18GENIChomozygous52160626
107088350270883503TA18GENIChomozygous52160627
107088356170883562CCTTTTTT2GENICheterozygous52384152
107088358070883590GCTTATTTGG----------8GENICheterozygous52384153
107088531070885311TC26GENIChomozygous51689636
107088584370885844TTG8GENIChomozygous51489575