chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124810587448105875TC53GENIChomozygous115345490
124810643748106438AG65GENIChomozygous115345492
124810648748106487G68GENIChomozygous128998459
124810691648106917AG75GENIChomozygous115345494
124810692848106929CT73GENIChomozygous115345496
124810982948109830AC58GENIChomozygous115345500
124811102748111028GC59GENIChomozygous115345504
124811195248111953CT70GENIChomozygous115398969
124810925148109252GA58GENIChomozygous115495807
124811058248110583CG46GENIChomozygous115398961
124811074948110750GA69GENIChomozygous115398963
124811119548111196CT58GENIChomozygous115398965
124811129948111300CT53GENIChomozygous115398967
124811296548112966TC77GENIChomozygous115345506
124811405748114058CT63GENIChomozygous115398971
124811466948114670GA57GENIChomozygous115345510
124811655548116556GA26GENIChomozygous115345512
124811710848117109CA58GENICpossibly homozygous115345514
124811747648117476G4GENIChomozygous130044497
124811356548113567TG53GENIChomozygous133766664
124811658148116585GGAG23GENIChomozygous133766665
124811724248117305ATGCACACACATACGCATGCACACACATACGCATGCACACACATACGCATGCACACACATACA30GENIChomozygous133766666
124811741248117413GA4GENIChomozygous118272944
124811747648117477AC4GENIChomozygous130049483
124811770048117700T11GENIChomozygous128998460
124812111848121119AT68GENIChomozygous115345518