chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120896291120896292GA33GENIChomozygous54860042
7120896593120896594TC18GENIChomozygous54860043
7120898171120898172TTAC13GENICheterozygous54085102
7120899319120899320CT38GENIChomozygous54860044
7120899849120899850A-14GENIChomozygous54587106
7120899978120899979G-7GENICheterozygous54085108
7120899980120899981G-7GENICheterozygous55030425
7120900188120900189AAAGAAAGAGAG9GENIChomozygous55001964
7120900227120900228GGAA10GENICpossibly homozygous55001966
7120900987120900988AAT14GENICpossibly homozygous55001968
7120901129120901130TTA10GENIChomozygous54860046
7120901687120901688GA26GENIChomozygous54860047
7120902123120902124G-18GENIChomozygous54860048
7120902134120902142ACAAAAAC--------25GENIChomozygous55001970
7120902183120902184GGA24GENIChomozygous54860049
7120903899120903900CCA10GENIChomozygous54860050
7120904214120904228TACACACACACACA--------------15GENIChomozygous54085130
7120909990120909991AG14GENIChomozygous54085153