chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157683346157683347TC40GENIChomozygous112906898
4157684503157684504CT24GENICpossibly homozygous113184577
4157685531157685532AC28GENIChomozygous113247249
4157685551157685552AG33GENICheterozygous113184579
4157685555157685556AG33GENICheterozygous113184580
4157685559157685560AG30GENICheterozygous113184581
4157686746157686747CG38GENIChomozygous112906902
4157690378157690379AG30GENIChomozygous112906906
4157690797157690798CT24GENIChomozygous112906908
4157694518157694519CT22GENIChomozygous113184582
4157695892157695893AG19GENIChomozygous113184583
4157696320157696321CT25GENICheterozygous113247250
4157699868157699869AT23GENIChomozygous113184584
4157703501157703502GA22GENIChomozygous113184585
4157705347157705348AG26GENIChomozygous113184586