chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
26660116566601166AG39GENICheterozygous109801019
26660117466601175CT37GENICheterozygous109801021
26660148666601487CT26GENIChomozygous110702251
26660160966601610AT28GENIChomozygous109801023
26660181766601818GA18GENIChomozygous109801026
26660186566601866TC19GENIChomozygous109801028
26660195966601960AG20GENIChomozygous109801030
26660750266607503CA30GENICheterozygous109801032
26660761566607616AG35GENIChomozygous109801034
26660764166607642TA39GENICheterozygous109801036
26660842266608423TA14GENIChomozygous109801046
26660906266609063CT15GENIChomozygous109801047
26660908266609083TC15GENIChomozygous109801049
26660936766609368AG32GENIChomozygous109801051
26660990966609910GA24GENIChomozygous109801053
26660994966609950CT27GENIChomozygous109801055
26661036566610366CA17GENIChomozygous109801057
26661038666610387TA15GENIChomozygous109801059
26661077266610773AG16GENIChomozygous109801061
26660889766608898GC18GENIChomozygous120124539
26661078166610782TA15GENIChomozygous120124540
26661081366610814GA11GENIChomozygous109801063
26661084366610844TA11GENIChomozygous109801065
26661226766612268AG20GENIChomozygous109801084
26661237666612377AG23GENIChomozygous109801086
26661253766612538CT22GENIChomozygous109801088
26661298166612982CT13GENIChomozygous109801090
26661304366613044CT7GENIChomozygous109801091
26661362866613629GA32GENIChomozygous109801095
26661432666614327GC33GENICpossibly homozygous109801101
26661456566614566AG32GENIChomozygous109801103
26661460666614607AG28GENIChomozygous109801105
26661492866614929AG31GENIChomozygous109801107