chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98274503582745036CT25GENICpossibly homozygous120456873
98274709982747100GT23GENIChomozygous120456874
98274899182748992CT21GENICpossibly homozygous120456875
98274935782749358TC24GENICpossibly homozygous120456876
98274948782749488AG29GENIChomozygous117589035
98275057182750572TC29GENICpossibly homozygous120280175
98275197682751977AG20GENIChomozygous120280176
98275237182752372CT28GENICpossibly homozygous120280177
98275279382752794CT30GENICpossibly homozygous120456877
98275328882753289TC28GENICpossibly homozygous120280178