chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107087247870872500GTGTGTGTGTGTGTGTGTGTGT----------------------20GENICpossibly homozygous52725066
107087280470872805AG27GENIChomozygous51489542
107087387570873876AG14GENIChomozygous51489543
107087387870873879TC14GENIChomozygous51489544
107087519170875192GGTTT14GENICheterozygous51489548
107087519170875192GGTT14GENICheterozygous51489549
107087540170875402AG22GENIChomozygous51489550
107087557170875577TGTGTA------10GENICheterozygous52725068
107087596370875964GA30GENIChomozygous52160618
107087609870876099TTG23GENIChomozygous52160619
107087616670876167GA29GENIChomozygous51689620
107087630770876308AG19GENIChomozygous51489555
107087637770876378CCAGG29GENIChomozygous51489556
107087658870876589TA19GENIChomozygous51489557
107087679170876792AAG24GENIChomozygous51489558
107087727970877280GA21GENIChomozygous51489559
107087770770877708AT20GENIChomozygous51689624
107087812270878123AATTCTTTCTTTCT4GENIChomozygous52725070
107087824670878247CT20GENIChomozygous52160621
107087899270878993GT26GENIChomozygous52160622
107088013870880140AA--9GENICpossibly homozygous51489566
107088013970880140A-9GENICheterozygous52384150
107088016170880162AG15GENIChomozygous51489567
107088152770881528GA19GENIChomozygous52160623
107088175670881757AG18GENIChomozygous52160624
107088263970882640GA26GENIChomozygous52160625
107088297670882977GA27GENIChomozygous52160626
107088350270883503TA28GENIChomozygous52160627
107088358070883590GCTTATTTGG----------4GENICheterozygous52384153
107088531070885311TC10GENIChomozygous51689636
107088584370885844TTG17GENICheterozygous51489575