chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15121550121551CT42GENIChomozygous112778874
15127756127757GT41GENIChomozygous112444139
15151047151048TG51GENICheterozygous119064904
15152660152661AG47GENICheterozygous118988304
15152678152679AG55GENICheterozygous119064905
15152732152733CG53GENIChomozygous112444142
15168547168548CG54GENICheterozygous119064906
15184219184220CG72GENICheterozygous119064907
15188725188726TG26GENICheterozygous119064908
15197111197112GA26GENIChomozygous112778987
15212140212141AG50GENICpossibly homozygous112779026
15214766214767TC50GENIChomozygous112779028
15229411229412TC41GENICpossibly homozygous112837441
15229780229781CA56GENIChomozygous112779072
15230205230206AG75GENIChomozygous112779075
15229742229743AC57GENIChomozygous113035412
15227187227188CT56GENICpossibly homozygous113035409