chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81297582212975823GC26GENICpossibly homozygous117090119
81297613812976139AG36GENIChomozygous117090120
81297618512976186CT29GENIChomozygous117090121
81297829312978294AG27GENIChomozygous117090124
81297904112979042AT25GENIChomozygous118057793
81297962212979623AG22GENIChomozygous117090125
81298068712980688GA39GENIChomozygous117090127
81298226712982268CT35GENIChomozygous117090129
81298417212984173GA18GENIChomozygous117090130
81298589512985896CT42GENIChomozygous118057794
81299149112991492GA46GENIChomozygous118057795