chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104418765644187657GA40GENICheterozygous117991662
104418767044187671GA41GENICheterozygous117991663
104418773044187731AC32GENICheterozygous117991664
104418793144187932AG25GENICheterozygous117991668
104418797644187977TG28GENICheterozygous117991669
104418798244187983TA28GENICheterozygous117991670
104418799544187996CT22GENICheterozygous117991671
104418805944188060GT26GENICheterozygous117991672
104418806244188063AG28GENICheterozygous117991673
104418807944188080TC37GENICheterozygous117991674
104418811844188119CT38GENICheterozygous117991675
104418817844188179GT34GENICheterozygous117991676
104418819944188200CT37GENICheterozygous117991677
104418829544188296CT37GENICheterozygous117991678
104418834944188350CT42GENICheterozygous116580598
104418842744188428GA42GENICheterozygous117058489