chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123916615139166152GT52GENICheterozygous118270173
123916625439166255GT6GENIChomozygous118270174
123916669739166698CA69GENICpossibly homozygous115324942
123916715739167158AG43GENIChomozygous115324944
123916728939167290CG30GENICpossibly homozygous115494058
123916776639167767GA32GENICpossibly homozygous115324946
123916830239168303GA58GENIChomozygous115324948
123916932339169324TC51GENIChomozygous118270175
123916937339169374TC40GENIChomozygous118304700
123916940239169403AG33GENIChomozygous118304701
123917183439171835AG35GENICpossibly homozygous115324964
123917230439172305TA31GENICpossibly homozygous115486247
123917448639174487TC4GENIChomozygous118270176
123917449039174491CG5GENIChomozygous118270177
123917449539174496CT7GENIChomozygous118270178
123917481339174814TC40GENIChomozygous118270179
123918332139183322CG40GENICpossibly homozygous115324972