chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101454911914549120TG17GENICpossibly homozygous116737085
101455262714552628TA10GENIChomozygous116496659
101455265114552652TC9GENIChomozygous116737086
101455781914557820AG12GENIChomozygous116496661
101455827114558272CT9GENIChomozygous116496663
101455972114559722AC11GENICheterozygous117294233
101456218214562183GA12GENIChomozygous116496665
101456377414563775GA23GENIChomozygous116496667
101456386214563863TC28GENIChomozygous116496669
101456565714565658TC24GENIChomozygous116496671
101456792014567921CT21GENIChomozygous116496675
101456793614567937AC21GENIChomozygous116496677
101457175414571755AG21GENIChomozygous116496685
101457194814571949GA14GENIChomozygous116496687
101457372214573723TC5GENIChomozygous116496695
101457599014575991AG23GENIChomozygous116496697
101457672814576729TG20GENIChomozygous116496699
101457797614577977GA18GENIChomozygous116496701
101457888314578884GT12GENIChomozygous116496703
101458144814581449CT16GENIChomozygous116496705
101458149614581497CT21GENIChomozygous116496707
101458155414581555AC29GENIChomozygous116496709
101458171314581714GT14GENICheterozygous117294235
101458224914582250TC23GENIChomozygous116496711
101458352514583526AG16GENIChomozygous116496713
101458378014583781TG28GENIChomozygous116496715
101458692414586925AG26GENIChomozygous116496717
101458695314586954TG26GENIChomozygous116496719
101458711214587113AC14GENIChomozygous116496721
101458757314587574TA25GENIChomozygous116496723
101458761914587620TC24GENIChomozygous116496725
101458767514587676GA28GENIChomozygous116496727
101458780314587804GA8GENIChomozygous116496729
101458783114587832TC8GENIChomozygous116496731
101458977914589780TG16GENIChomozygous116496733