chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1222538559222538560CT39GENICpossibly homozygous109449776
1222542059222542060TC27GENIChomozygous109449777
1222544373222544374GA24GENIChomozygous109449778
1222545124222545125AG21GENIChomozygous108546829
1222545750222545751CT35GENIChomozygous108546830
1222555784222555785GT24GENIChomozygous108546836
1222560714222560715TC23GENIChomozygous108770300
1222561018222561019AG29GENIChomozygous108546838
1222561499222561500GC20GENIChomozygous108546840
1222564566222564567AG37GENIChomozygous108546842
1222565993222565994GA25GENIChomozygous108546844
1222566638222566639TG25GENICpossibly homozygous108546846
1222571183222571184CT17GENICpossibly homozygous108546850