chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
26092883160928832AC18GENIChomozygous60212349
26092988660929887TC16GENICpossibly homozygous59810849
26093043960930440GT23GENIChomozygous60212350
26093054760930548AG27GENICpossibly homozygous59810850
26093116360931164TG13GENICheterozygous60212351
26093121160931212AT20GENICpossibly homozygous59810854
26093141460931415TG21GENIChomozygous60212352
26093169360931694AG8GENIChomozygous60113536
26093172160931722AT13GENIChomozygous60113537
26093174360931744TA9GENICpossibly homozygous59810855
26093189860931899TC20GENICpossibly homozygous59810856
26093296560932966TC13GENIChomozygous60212353
26093311160933112AC9GENIChomozygous59810863
26093325960933260CT25GENIChomozygous59810864