chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152502401152502402TC43GENICheterozygous56986210
4152502404152502405CT43GENICheterozygous57842908
4152502450152502451GT13GENICheterozygous57349540
4152502453152502454AT22GENICheterozygous57349542
4152502462152502463AG25GENICheterozygous57349544
4152502463152502464AG26GENICheterozygous57349546
4152502474152502475AG34GENICheterozygous57349548
4152502476152502477AG38GENICheterozygous57349550
4152502477152502478AT37GENICheterozygous57349552
4152502512152502513GA62GENICheterozygous57349554
4152502521152502522CA67GENICheterozygous57842909
4152503011152503012GA99GENICheterozygous57842910
4152503049152503050GC104GENICheterozygous57842911
4152503058152503059GA99GENICheterozygous56986211
4152506653152506654TTA2GENICheterozygous57842912
4152506663152506664CCA2GENIChomozygous56986215
4152506685152506686AG22GENICpossibly homozygous57842913
4152506692152506693TA26GENIChomozygous56986216
4152506724152506726TT--34GENIChomozygous57842914
4152506994152506995TA31GENICpossibly homozygous57842915
4152507155152507156CG35GENIChomozygous57842916