chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1240978336240978337TG20GENICpossibly homozygous120889759
1240979490240979491AG26GENICpossibly homozygous109540727
1240980950240980951CT19GENICpossibly homozygous120889760
1240981424240981425TC11GENIChomozygous120889761
1240987538240987539CA34GENICpossibly homozygous120889762
1240988031240988032CT22GENIChomozygous120818572
1240988056240988057CT27GENIChomozygous109540730
1240990771240990772CT33GENICpossibly homozygous120889763
1240991737240991738AG26GENICpossibly homozygous109540732
1241001372241001373TC25GENIChomozygous120684647
1241001602241001603GT26GENICpossibly homozygous120684649
1241003249241003250TC30GENIChomozygous109540737
1241003401241003402TC13GENIChomozygous109540738
1241006379241006380GA26GENICpossibly homozygous120889764
1241009388241009389GA20GENIChomozygous120889765
1241009389241009390CA20GENIChomozygous120889766
1241009788241009789GA13GENICheterozygous120889767
1241010054241010055TC24GENICpossibly homozygous120889768
1241014962241014963GA20GENICpossibly homozygous120889769
1241019700241019701AG16GENIChomozygous109540742
1241019716241019717CG11GENIChomozygous109540743
1241020986241020987GA29GENIChomozygous120889771
1241021415241021416AT24GENIChomozygous109540745
1241025577241025578CA34GENICpossibly homozygous120889772
1241025636241025637AC34GENICpossibly homozygous120684667
1241029214241029215TC25GENIChomozygous120684669
1241030144241030145TC27GENIChomozygous120684675
1241035885241035886TA14GENICheterozygous120902573
1241035886241035887TA14GENICheterozygous120902574
1241035887241035888TA21GENICpossibly homozygous120902575
1241041015241041016TA16GENICheterozygous120902576
1241041022241041023GA17GENICheterozygous120902577
1241044710241044711AG26GENIChomozygous120684685