chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1119058051905806GC22GENIChomozygous118133075
1119058451905846GA15GENIChomozygous118133076
1119084561908457GC8GENIChomozygous118133077
1119085751908576GC15GENICpossibly homozygous118133078
1119148031914804GA21GENICheterozygous118133080
1119148121914813TA21GENICheterozygous118133081
1119148171914818TC22GENICheterozygous118133082
1119148201914821TC21GENICheterozygous118133083
1119148461914847TC23GENICheterozygous118133084