chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101455262714552628TA21GENIChomozygous116496659
101455265114552652TC18GENIChomozygous116737086
101455781914557820AG38GENIChomozygous116496661
101455827114558272CT18GENIChomozygous116496663
101456218214562183GA33GENIChomozygous116496665
101456377414563775GA21GENIChomozygous116496667
101456386214563863TC24GENIChomozygous116496669
101456565714565658TC24GENIChomozygous116496671
101456651914566520AC10GENIChomozygous116496673
101456792014567921CT32GENIChomozygous116496675
101456793614567937AC32GENIChomozygous116496677
101457175414571755AG22GENIChomozygous116496685
101457194814571949GA23GENIChomozygous116496687
101457364614573647TA10GENIChomozygous116496689
101457367614573677TC4GENIChomozygous116496691
101457367814573679TC4GENIChomozygous116496693
101457372214573723TC8GENIChomozygous116496695
101457599014575991AG21GENICpossibly homozygous116496697
101457672814576729TG42GENIChomozygous116496699
101457797614577977GA32GENIChomozygous116496701
101457888314578884GT26GENIChomozygous116496703
101458144814581449CT22GENIChomozygous116496705
101458149614581497CT19GENIChomozygous116496707
101458155414581555AC17GENIChomozygous116496709
101458224914582250TC33GENIChomozygous116496711
101458352514583526AG27GENIChomozygous116496713
101458378014583781TG24GENIChomozygous116496715
101458692414586925AG24GENIChomozygous116496717
101458695314586954TG26GENIChomozygous116496719
101458711214587113AC40GENIChomozygous116496721
101458757314587574TA34GENIChomozygous116496723
101458761914587620TC31GENIChomozygous116496725
101458767514587676GA26GENIChomozygous116496727
101458780314587804GA48GENIChomozygous116496729
101458783114587832TC48GENIChomozygous116496731