chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144250450144250451CT20GENIChomozygous114254001
5144251154144251155AC13GENIChomozygous114036846
5144251656144251657CT23GENIChomozygous114036847
5144252465144252466TC13GENIChomozygous114036848
5144252497144252498GA11GENIChomozygous114036849
5144253315144253316TG7GENIChomozygous114152289
5144253444144253445AC8GENIChomozygous114036851
5144254476144254477AG24GENIChomozygous114152295
5144254611144254612AG18GENIChomozygous114152296
5144254697144254698TG19GENIChomozygous114152297
5144255307144255308GA23GENIChomozygous114649989
5144254236144254237GA14GENIChomozygous114649985
5144254587144254588GA18GENIChomozygous114649987
5144257257144257258AG16GENIChomozygous114152299
5144257337144257338GA24GENIChomozygous114152300
5144258211144258212AC33GENIChomozygous114649993
5144258308144258309GT26GENIChomozygous114649995
5144258737144258738AG10GENIChomozygous114152301
5144258833144258834AC4GENIChomozygous119054621
5144259480144259481TC27GENIChomozygous114036860
5144261703144261704TC20GENIChomozygous114036865
5144266620144266621TC2GENIChomozygous118912367
5144268331144268332GA11GENIChomozygous114649997
5144268761144268762CT16GENIChomozygous114036880
5144268923144268924GT30GENIChomozygous114036881
5144269121144269122CT16GENIChomozygous114036882
5144270110144270111GA22GENIChomozygous114152305
5144270839144270840GA15GENIChomozygous114649999
5144270961144270962GC13GENIChomozygous114036885
5144271080144271081CT16GENIChomozygous114036886
5144272480144272481CA17GENIChomozygous114152307
5144274216144274217CT7GENIChomozygous114650001
5144266373144266374AT5GENIChomozygous114445824