chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144250450144250451CT27GENIChomozygous114254001
5144250950144250951AG28GENIChomozygous114036843
5144251154144251155AC33GENIChomozygous114036846
5144251656144251657CT24GENIChomozygous114036847
5144252465144252466TC36GENIChomozygous114036848
5144252497144252498GA37GENIChomozygous114036849
5144253315144253316TG31GENIChomozygous114152289
5144253444144253445AC23GENICpossibly homozygous114036851
5144253538144253539AG5GENIChomozygous114152290
5144253569144253570TC3GENIChomozygous114152291
5144254103144254104TC22GENIChomozygous114036853
5144254476144254477AG37GENIChomozygous114152295
5144254611144254612AG29GENIChomozygous114152296
5144254697144254698TG24GENIChomozygous114152297
5144255307144255308GA46GENIChomozygous114649989
5144254236144254237GA51GENIChomozygous114649985
5144254587144254588GA29GENIChomozygous114649987
5144255945144255946GA38GENIChomozygous114649991
5144257257144257258AG30GENIChomozygous114152299
5144257337144257338GA28GENIChomozygous114152300
5144258211144258212AC48GENICpossibly homozygous114649993
5144258308144258309GT37GENIChomozygous114649995
5144258737144258738AG3GENIChomozygous114152301
5144259480144259481TC28GENIChomozygous114036860
5144261703144261704TC49GENIChomozygous114036865
5144268331144268332GA21GENIChomozygous114649997
5144268761144268762CT32GENIChomozygous114036880
5144268923144268924GT35GENIChomozygous114036881
5144269121144269122CT37GENIChomozygous114036882
5144270110144270111GA33GENIChomozygous114152305
5144270839144270840GA40GENIChomozygous114649999
5144274216144274217CT23GENIChomozygous114650001
5144270961144270962GC25GENIChomozygous114036885
5144271080144271081CT25GENIChomozygous114036886
5144272480144272481CA33GENIChomozygous114152307
5144273800144273801GT28GENICheterozygous114036889