chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157683346157683347TC18GENIChomozygous112906898
4157684503157684504CT13GENIChomozygous113184577
4157685539157685540AG27GENICheterozygous113184578
4157685551157685552AG31GENICheterozygous113184579
4157685555157685556AG32GENICheterozygous113184580
4157685559157685560AG32GENICheterozygous113184581
4157686746157686747CG27GENIChomozygous112906902
4157690378157690379AG17GENIChomozygous112906906
4157690797157690798CT22GENIChomozygous112906908
4157694518157694519CT37GENIChomozygous113184582
4157695892157695893AG28GENIChomozygous113184583
4157699868157699869AT24GENIChomozygous113184584
4157703501157703502GA26GENIChomozygous113184585
4157705347157705348AG26GENIChomozygous113184586