chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42997681529976816TC15GENIChomozygous112567559
42997687429976875TG12GENIChomozygous112567561
42997716129977161A35GENICpossibly homozygous128018952
43000545930005460TG23GENICheterozygous112567563
43000545930005459G22GENICheterozygous131640661
43006496330064964CG30GENICheterozygous113004144
43006496530064966GC30GENICheterozygous113004146
43006620530066206GC5GENICheterozygous133951962
43000546030005461TG23GENICheterozygous119303619
43006530430065305CT14GENICheterozygous128121293
43006523830065239TG10GENICheterozygous129907263
43006606030066061TA13GENICheterozygous133731611
43009631130096312TC4GENIChomozygous128121296
43009633430096335T4GENIChomozygous128018953
43009634830096349AG4GENIChomozygous128121297
43013410830134110GT18GENICheterozygous128018955
43016413830164141CCT3GENICheterozygous130648223
43016415630164157TC4GENICheterozygous130650706
43017164030171642AT32GENICheterozygous128018958
43022831130228313TG32GENICheterozygous130294222
43023795930237960T44GENICheterozygous128018959
43016416030164161TC6GENICheterozygous134686053