chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124342323643423237CCAAACAAAACAAAACA20GENIChomozygous50544674
124342367643423678CC--15GENIChomozygous50384063
124342433043424331CT26GENIChomozygous50453093
124342472843424729TC33GENIChomozygous50453094
124342557743425579AC--14GENIChomozygous50384064
124342589143425892GA23GENIChomozygous50384065
124342609843426099GGAAAAAAAAAAAAA8GENICheterozygous50544675
124342703543427036TC20GENIChomozygous50211731
124342750043427508CACACACA--------14GENICpossibly homozygous50329825
124343107543431076GGACAC2GENIChomozygous50544676
124343209943432100CT31GENIChomozygous50453095
124343313543433136AC15GENIChomozygous50211821
124343323943433240GGACTTACTT10GENIChomozygous50544678
124343360143433602TA12GENIChomozygous50211825
124343518643435187AG28GENIChomozygous50384070
124343621543436216TC22GENIChomozygous50211838
124343673143436732CCT9GENICheterozygous50544679
124343673143436732CCTT9GENICheterozygous50572639
124343784343437844AAACACAC4GENICheterozygous50211841
124343784343437844AAACACACACAC4GENICheterozygous50544680
124343907543439076AAG33GENIChomozygous50211844
124343941943439420GGCA6GENICheterozygous50329863
124344021343440214GA31GENIChomozygous50211846
124344030143440302AG37GENIChomozygous50329865
124344055543440556TC31GENIChomozygous50211848
124344088743440888CT34GENIChomozygous50329868
124344100343441004AG22GENIChomozygous50329870
124344106743441068CT24GENIChomozygous50329872
124344118243441183CT17GENIChomozygous50329874
124344130043441306ACACAC------6GENICheterozygous50544683
124344130243441306ACAC----6GENICheterozygous50544684
124344134643441347A-10GENIChomozygous50329876
124344139543441396TA20GENIChomozygous50211850
124344153743441538C-3GENIChomozygous50329880
124344285643442857TTCTA26GENIChomozygous50329882
124344288943442890AAT14GENICpossibly homozygous50211854
124344356843443569GGT23GENIChomozygous50329884