chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120387249120387250GA26GENIChomozygous54084081
7120387941120387942TC15GENICheterozygous54084082
7120388694120388695AG17GENIChomozygous54084083
7120389509120389510CT7GENICheterozygous54084084
7120389607120389608AG16GENIChomozygous54084085
7120389713120389714AG25GENIChomozygous54084086
7120390296120390297AG24GENIChomozygous54084087
7120390335120390336GA19GENIChomozygous54084088
7120390388120390389GC20GENIChomozygous54084089
7120390852120390853CT26GENICpossibly homozygous54084090
7120390927120390928TC12GENIChomozygous54084091
7120391170120391171AG11GENIChomozygous54084092
7120391780120391781AG17GENIChomozygous54084093
7120392222120392223GA27GENICpossibly homozygous54084094
7120392714120392715CT22GENICpossibly homozygous54084095
7120393749120393750TC14GENIChomozygous54084096
7120394797120394798TC8GENIChomozygous54084098
7120394923120394924TC16GENICheterozygous54084099
7120394944120394945TG14GENICpossibly homozygous54084100
7120395441120395442TC12GENICpossibly homozygous54084101