chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104343588643435886C9GENIChomozygous128812868
104343590043435900G11GENIChomozygous128812869
104343600543436005C7GENIChomozygous128812870
104343602743436027G6GENIChomozygous128812871
104344797443447975G45GENIChomozygous130776709
104344808243448083GC23GENIChomozygous123350394
104344909843449099AC53GENIChomozygous123350397
104344717843447179TC44GENIChomozygous116766314
104344881343448814GA50GENIChomozygous116766318
104345054943450550GA57GENIChomozygous116766322
104344810743448108AG23GENIChomozygous117128316
104344887243448873AT59GENIChomozygous116875757
104344906543449065C53GENICpossibly homozygous131092285
104344967743449678GA63GENIChomozygous116578837
104345545643455457C54GENIChomozygous128812872
104345757843457586AGTCAGTC37GENIChomozygous131092286
104345846843458469GA68GENICpossibly homozygous116875759
104345884143458842TA65GENIChomozygous116875761
104346016943460170G11GENICheterozygous128812873
104346017243460172TATATG12GENICheterozygous128812874
104346062243460622A49GENIChomozygous128812875
104346439943464399A48GENIChomozygous128812876
104347019143470228TACCTACTTTCTTAATTGATTGTGAAACACTATTGGG44GENIChomozygous128812877
104347595443475954C54GENIChomozygous131092287
104346232643462327TG3GENIChomozygous134437655
104346233043462331TG3GENIChomozygous128868359
104347913743479138TG61GENIChomozygous116875763
104348095343480953G38GENIChomozygous128812878
104349312943493129C58GENIChomozygous128812879
104349326343493264T63GENIChomozygous128812880
104349329743493299CC73GENIChomozygous128812881
104349333043493331CT66GENIChomozygous116578843
104349441143494412AG6GENIChomozygous116578845
104349442643494427TG10GENIChomozygous116578847
104349506943495070CT71GENIChomozygous116875765
104349863043498630A12GENIChomozygous131092288
104350004543500046TC63GENIChomozygous116766374